Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 12:49578118 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.49578118C>T

Variation displays