Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y
Location

Chromosome 12:52863074 (forward strand) | View in location tab

Co-located

with dbSNP rs11540295 (C/T)

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Variation displays