Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome X:37779094 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58670136

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2 sample genotypes.

Variant displays