Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.26 (T)
Location

Chromosome 2:138787007 (forward strand)|View in location tab

Most severe consequence
 
Regulatory region variant
Evidence status

Synonyms

Archive dbSNP rs57317930

HGVS name

2:g.138787007C>T

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 4026 sample genotypes and is mentioned in 2 citations.

Variant displays