Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M
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

About this variant

This variant overlaps 7 transcripts and has 1186 individual genotypes.

Variation displays