Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 11:62690071 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.62690071T>C

Variation displays