Original source

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

Alleles
A/G | Ambiguity code: R
Location

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

Co-located

with HGMD-PUBLIC CM073198

Most severe consequence
Evidence status

Clinical significance

Synonyms

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

This variation has 7 HGVS names - click the plus to show

About this variant

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

Variation displays