Original source

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

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

Chromosome 11:636047 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.636047T>C

Variation displays