Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.48 (C)
Location

Chromosome 2:9557243 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs36217005

HGVS name

2:g.9557243A>C

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 3691 sample genotypes and is mentioned in 4 citations.

Variant displays