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rs267607072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607072(A;T)
Make rs267607072(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position23787261
GeneSMARCB1
is asnp
is mentioned by
dbSNPrs267607072
ebirs267607072
HLIrs267607072
Exacrs267607072
Varsomers267607072
Maprs267607072
PheGenIrs267607072
hapmaprs267607072
1000 genomesrs267607072
hgdprs267607072
ensemblrs267607072
gopubmedrs267607072
geneviewrs267607072
scholarrs267607072
googlers267607072
pharmgkbrs267607072
gwascentralrs267607072
openSNPrs267607072
23andMers267607072
23andMe allrs267607072
SNP Nexus

SNPshotrs267607072
SNPdbers267607072
MSV3drs267607072
GWAS Ctlgrs267607072
Max Magnitude0
ClinVar
Risk rs267607072(T;T)
Alt rs267607072(T;T)
Reference rs267607072(A;A)
Significance Pathogenic
Disease SCHWANNOMATOSIS 1
Variation info
Gene SMARCB1
CLNDBN SCHWANNOMATOSIS 1
Reversed 0
HGVS NC_000022.10:g.24129448A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008496.4,