Have questions? Visit https://www.reddit.com/r/SNPedia

rs878854224

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854224(C;T)
Make rs878854224(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11041379
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs878854224
ebirs878854224
HLIrs878854224
Exacrs878854224
Varsomers878854224
Maprs878854224
PheGenIrs878854224
hapmaprs878854224
1000 genomesrs878854224
hgdprs878854224
ensemblrs878854224
gopubmedrs878854224
geneviewrs878854224
scholarrs878854224
googlers878854224
pharmgkbrs878854224
gwascentralrs878854224
openSNPrs878854224
23andMers878854224
23andMe allrs878854224
SNP Nexus

SNPshotrs878854224
SNPdbers878854224
MSV3drs878854224
GWAS Ctlgrs878854224
Max Magnitude0
ClinVar
Risk rs878854224(T;T)
Alt rs878854224(T;T)
Reference rs878854224(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.11152055C>T
CLNSRC
CLNACC RCV000232997.1,