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rs267607070

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607070(C;T)
Make rs267607070(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position11033308
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs267607070
ebirs267607070
HLIrs267607070
Exacrs267607070
Varsomers267607070
Maprs267607070
PheGenIrs267607070
hapmaprs267607070
1000 genomesrs267607070
hgdprs267607070
ensemblrs267607070
gopubmedrs267607070
geneviewrs267607070
scholarrs267607070
googlers267607070
pharmgkbrs267607070
gwascentralrs267607070
openSNPrs267607070
23andMers267607070
23andMe allrs267607070
SNP Nexus

SNPshotrs267607070
SNPdbers267607070
MSV3drs267607070
GWAS Ctlgrs267607070
Max Magnitude0
ClinVar
Risk rs267607070(T;T)
Alt rs267607070(T;T)
Reference rs267607070(C;C)
Significance Pathogenic
Disease Rhabdoid tumor predisposition syndrome 2
Variation info
Gene SMARCA4
CLNDBN Rhabdoid tumor predisposition syndrome 2
Reversed 0
HGVS NC_000019.9:g.11143984C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006932.3,