Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.30 (C)

Chromosome 12:20846134 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs74234843

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2778 sample genotypes.

Variant displays