Original source

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

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.50 (C)
Location

Chromosome 12:109787117 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58015411

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 8 transcripts and has 3655 sample genotypes.

Variant displays