Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.26 (T)
Location

Chromosome X:46770843 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs6521168, rs57397176

HGVS name

X:g.46770843T>C

Variation displays