Original source

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

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

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

Co-located variant

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