Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 7:101126005 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.101126005C>T

About this variant

This variant overlaps 1 transcript and has 2551 individual genotypes.

Variation displays