Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome X:151395949 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58595309

HGVS name

X:g.151395949C>G

About this variant

This variant overlaps 3 transcripts and has 7 individual genotypes.

Variation displays