Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.14 (T)
Location

Chromosome 7:38976055 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.38976055A>T

About this variant

This variant overlaps 2 transcripts and has 2771 individual genotypes.

Variation displays