Original source

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

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

Chromosome X:3604131 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60597162

HGVS name

X:g.3604131G>C

About this variant

This variant overlaps 3 transcripts and has 7 individual genotypes.

Variation displays