Original source

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

C/G | Ancestral: C | Ambiguity code: S

Chromosome 12:7694464 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs5013153

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2510 sample genotypes.

Variant displays