Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 7 chips - click the plus to show

About this variant

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

Variant displays