Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.44 (T)
Location

Chromosome 1:47414121 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.47414121T>C

Variation displays