Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:46837176 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981711

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_316_RP2_312600_0002, 7845

This variation has 3 HGVS names - click the plus to show

X:g.46837176C>T
ENST00000218340.3:c.76C>T
ENSP00000218340.3:p.Gln26Ter

Variation displays