Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome X:71127367 (forward strand) | View in location tab

Co-located

with COSMIC COSM1319413 (C/T), COSM1319414 (C/T) ; HGMD-PUBLIC CM071860

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6887, NM_005120.2:c.2881C>T

This variation has 9 HGVS names - click the plus to show

Variation displays