Original source

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

T/A/G | Ancestral: G | Ambiguity code: D

Chromosome 12:7694435 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61238066

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 6 sample genotypes.

Variant displays