Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.04 (A)

Chromosome 12:48772216 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3729971

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 2769 sample genotypes and is mentioned in 1 citation.

Variant displays