Establish The Correct Gene(s) – Variant Pairs Using A Genome Browser; Variants May Also Be Located Outside A Gene; Typically, The Nearest Gene(s) To This Variant Will Be Included In The List. Obtain A Reference Sequence (rs) Id For All Variants. ~ TheNursingWriter.com

Establish the correct gene(s) – variant pairs using a genome browser; variants may also be located outside a gene; typically, the nearest gene(s) to this variant will be included in the list. Obtain a reference sequence (rs) id for all variants.
Use database resources to explore what is known about the function of each gene and the protein it encodes (i.e. a few sentences summarising what the gene does) as well as its tissue expression profile. Prepare a table with each gene’s potential implication to disease.
Establish the functional impact of each sequence variant; for example, is a variant located in a coding region of the genome and if yes, does it alter an amino acid? or is it overlapping a regulatory element? Report this element e.g. promoter
Are there any good proxy SNPs (r² ≥ 0.8) for the variants rs7636 and rs13107325?
Report, where possible, the minor allele frequency of each variant in the population – reference the data source you used (e.g. URL of data base or repository). Use a database to report MAF in different population groups i.e. HapMap / 1000Genomes panels. Discuss if you observe any frequency differences between populations.
Investigate using both variant identifier and the gene name whether there is a known association to one or more human traits (e.g. blood pressure) including disease.
For those genes you have established an association to a human trait(s) report the number of known rare variants and how many of these rare variants are Loss of Function.
Does rs13107325 have any unusual features in terms of its LD relationship to other nearby common variants in European-descent populations? In which common diseases this variant may play a role?
Based on all the information assembled, assess whether the genes found in question 1 could be divided in to subgroups underlying a specific trait or combination of traits.
Are there any epigenetic effects known to be associated with the trait(s) of the subgroup(s) you defined (i.e. question 9)

gene name	DNA Sequence variant
ACHE	rs2145270
ALDOA	rs6235
ANAPC4	rs10146997
BCL7A	rs1064395
BMP2	rs10838738
BPTF	rs11546878
C6orf106	rs11835818
CASC20	rs12602912
CYB5B	rs13107325
DNAJC27	rs141845046
ECE2	3:185529080
GIPC2	1:78623626
IGF2BP2	rs17782313
LOXL4	rs1983864
MC4R	rs2814993
MIR1538	rs34811474
MTCH2	rs4665736
NCAN	rs4783718
NRXN3	rs7636
PCCB	rs9844666
PCSK1	rs9928448
SLC39A8
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Establish the correct gene(s) – variant pairs using a genome browser; variants may also be located outside a gene; typically, the nearest gene(s) to this variant will be included in the list. Obtain a reference sequence (rs) id for all variants.

Establish the correct gene(s) – variant pairs using a genome browser; variants may also be located outside a gene; typically, the nearest gene(s) to this variant will be included in the list. Obtain a reference sequence (rs) id for all variants.