Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.44 (C)
Location

Chromosome 12:21839190 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58283879, rs1688472

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2779 sample genotypes.

Variant displays