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rs267607076

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607076(G;G)
Make rs267607076(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position21977126
GeneSMS
is asnp
is mentioned by
dbSNPrs267607076
ebirs267607076
HLIrs267607076
Exacrs267607076
Varsomers267607076
Maprs267607076
PheGenIrs267607076
hapmaprs267607076
1000 genomesrs267607076
hgdprs267607076
ensemblrs267607076
gopubmedrs267607076
geneviewrs267607076
scholarrs267607076
googlers267607076
pharmgkbrs267607076
gwascentralrs267607076
openSNPrs267607076
23andMers267607076
23andMe allrs267607076
SNP Nexus

SNPshotrs267607076
SNPdbers267607076
MSV3drs267607076
GWAS Ctlgrs267607076
Max Magnitude0
ClinVar
Risk rs267607076(G;G)
Alt rs267607076(G;G)
Reference rs267607076(T;T)
Significance Pathogenic
Disease Snyder Robinson syndrome
Variation info
Gene SMS
CLNDBN Snyder Robinson syndrome
Reversed 0
HGVS NC_000023.10:g.21995244T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012391.25,