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 17:43755612 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010454

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13377, 2010_April_001_212_SOST_605740_0003

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

17:g.43755612C>T
ENST00000301691.2:c.372G>A
ENSP00000301691.1:p.Trp124Ter

Variation displays