Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.24 (T)
Location

Chromosome 1:116908411 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.116908411C>T

Variation displays