Original source

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

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.27 (A)
Location

Chromosome 12:132629721 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs6560892, rs59140641

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2511 sample genotypes.

Variant displays