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rs387906811

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906811(C;T)
Make rs387906811(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position23791805
GeneSMARCB1
is asnp
is mentioned by
dbSNPrs387906811
ebirs387906811
HLIrs387906811
Exacrs387906811
Varsomers387906811
Maprs387906811
PheGenIrs387906811
hapmaprs387906811
1000 genomesrs387906811
hgdprs387906811
ensemblrs387906811
gopubmedrs387906811
geneviewrs387906811
scholarrs387906811
googlers387906811
pharmgkbrs387906811
gwascentralrs387906811
openSNPrs387906811
23andMers387906811
23andMe allrs387906811
SNP Nexus

SNPshotrs387906811
SNPdbers387906811
MSV3drs387906811
GWAS Ctlgrs387906811
Max Magnitude0
ClinVar
Risk rs387906811(T;T)
Alt rs387906811(T;T)
Reference rs387906811(C;C)
Significance Pathogenic
Disease SCHWANNOMATOSIS 1
Variation info
Gene SMARCB1
CLNDBN SCHWANNOMATOSIS 1
Reversed 0
HGVS NC_000022.10:g.24133992C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023122.5,