Original source

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

C/A|Ancestral: A|Ambiguity code: M|MAF: 0.40 (C)

Chromosome 12:112439796 (forward strand)|View in location tab

Co-located variant

dbSNP rs201900443 (C/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59650159

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2507 sample genotypes.

Variant displays