Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.12 (A)
Location

Chromosome 7:38976998 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

7:g.38976998T>A

About this variant

This variant overlaps 1 transcript and has 2505 sample genotypes.

Variant displays