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: 0.30 (T)
Location

Chromosome X:120426744 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58259470, rs3174393

HGVS name

X:g.120426744T>C

Variation displays