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rs397515549

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515549(A;A)
Make rs397515549(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position21971900
GeneSMS
is asnp
is mentioned by
dbSNPrs397515549
ebirs397515549
HLIrs397515549
Exacrs397515549
Varsomers397515549
Maprs397515549
PheGenIrs397515549
hapmaprs397515549
1000 genomesrs397515549
hgdprs397515549
ensemblrs397515549
gopubmedrs397515549
geneviewrs397515549
scholarrs397515549
googlers397515549
pharmgkbrs397515549
gwascentralrs397515549
openSNPrs397515549
23andMers397515549
23andMe allrs397515549
SNP Nexus

SNPshotrs397515549
SNPdbers397515549
MSV3drs397515549
GWAS Ctlgrs397515549
Max Magnitude0
ClinVar
Risk rs397515549(A;A)
Alt rs397515549(A;A)
Reference rs397515549(T;T)
Significance Pathogenic
Disease Snyder Robinson syndrome
Variation info
Gene SMS
CLNDBN Snyder Robinson syndrome
Reversed 0
HGVS NC_000023.10:g.21990018T>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000055902.1,