Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.48 (A)
Location

Chromosome X:48529077 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57410751

HGVS name

X:g.48529077A>C

This variation has assays on 6 chips - click the plus to show

Variation displays