Original source

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

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

Chromosome X:135227204 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.135227204C>T

Variation displays