Original source

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

C/A | Ambiguity code: M | MAF: 0.45 (C)

Chromosome 7:76416816 (forward strand) | View in location tab


with dbSNP rs66795691 (ATA/CTC)

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2505 sample genotypes.

Variant displays