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rs397515551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515551(A;G)
Make rs397515551(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position21977174
GeneSMS
is asnp
is mentioned by
dbSNPrs397515551
ebirs397515551
HLIrs397515551
Exacrs397515551
Varsomers397515551
Maprs397515551
PheGenIrs397515551
hapmaprs397515551
1000 genomesrs397515551
hgdprs397515551
ensemblrs397515551
gopubmedrs397515551
geneviewrs397515551
scholarrs397515551
googlers397515551
pharmgkbrs397515551
gwascentralrs397515551
openSNPrs397515551
23andMers397515551
23andMe allrs397515551
SNP Nexus

SNPshotrs397515551
SNPdbers397515551
MSV3drs397515551
GWAS Ctlgrs397515551
Max Magnitude0
ClinVar
Risk rs397515551(G;G)
Alt rs397515551(G;G)
Reference rs397515551(A;A)
Significance Pathogenic
Disease Snyder Robinson syndrome
Variation info
Gene SMS
CLNDBN Snyder Robinson syndrome
Reversed 0
HGVS NC_000023.10:g.21995292A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000055905.2,