Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | 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

Variation displays