Original source

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

Alleles
T/C | Ambiguity code: Y | MAF: 0.36 (C)
Location

Chromosome 12:52305764 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17126496, rs3741735

This variation has 3 HGVS names - click the plus to show

Variation displays