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rs587777463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777463(C;G)
Make rs587777463(G;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position11021722
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs587777463
ebirs587777463
HLIrs587777463
Exacrs587777463
Varsomers587777463
Maprs587777463
PheGenIrs587777463
hapmaprs587777463
1000 genomesrs587777463
hgdprs587777463
ensemblrs587777463
gopubmedrs587777463
geneviewrs587777463
scholarrs587777463
googlers587777463
pharmgkbrs587777463
gwascentralrs587777463
openSNPrs587777463
23andMers587777463
23andMe allrs587777463
SNP Nexus

SNPshotrs587777463
SNPdbers587777463
MSV3drs587777463
GWAS Ctlgrs587777463
Max Magnitude0
ClinVar
Risk rs587777463(G;G)
Alt rs587777463(G;G)
Reference rs587777463(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.11132398C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128405.3,