Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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