Original source

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

Alleles
A/G|Ambiguity code: R
Location

Chromosome X:71127931 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM073198

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 6888, NM_005120.2:c.3020A>G

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays