Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.17 (G)
Location

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

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60597162

HGVS name

X:g.3604131G>C

About this variant

This variant overlaps 3 transcripts and has 2511 sample genotypes.

Variant displays