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rs397515381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515381(A;A)
Make rs397515381(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position21972576
GeneSMS
is asnp
is mentioned by
dbSNPrs397515381
ebirs397515381
HLIrs397515381
Exacrs397515381
Varsomers397515381
Maprs397515381
PheGenIrs397515381
hapmaprs397515381
1000 genomesrs397515381
hgdprs397515381
ensemblrs397515381
gopubmedrs397515381
geneviewrs397515381
scholarrs397515381
googlers397515381
pharmgkbrs397515381
gwascentralrs397515381
openSNPrs397515381
23andMers397515381
23andMe allrs397515381
SNP Nexus

SNPshotrs397515381
SNPdbers397515381
MSV3drs397515381
GWAS Ctlgrs397515381
Max Magnitude0
ClinVar
Risk rs397515381(A;A)
Alt rs397515381(A;A)
Reference rs397515381(G;G)
Significance Pathogenic
Disease Snyder Robinson syndrome
Variation info
Gene SMS
CLNDBN Snyder Robinson syndrome
Reversed 0
HGVS NC_000023.10:g.21990694G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012389.15,