Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/A | Ancestral: A | Ambiguity code: M
Location

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

Co-located

with dbSNP rs201900443 (C/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59650159

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

Variation displays