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:48684350 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.48684350C>T

Variation displays