Original source

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

C/A | Ancestral: A | Ambiguity code: M | MAF: 0.25 (C)

Chromosome 19:10177755 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60730921

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2512 sample genotypes.

Variant displays