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 X:46911331 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.46911331T>C

Variation displays