Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome X:46770302 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.46770302C>T

Variation displays