Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with dbSNP rs201900443 (C/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59650159

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2507 sample genotypes.

Variant displays