Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.39 (C)
Location

Chromosome 12:132683334 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2595 sample genotypes.

Variant displays