Original source

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

Alleles
T/-|Ancestral: T|MAF: 0.03 (-)
Location

Chromosome 12:12715467 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs369210266, rs142904407

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays