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rs587777460

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777460(A;A)
Make rs587777460(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position11030880
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs587777460
ebirs587777460
HLIrs587777460
Exacrs587777460
Varsomers587777460
Maprs587777460
PheGenIrs587777460
hapmaprs587777460
1000 genomesrs587777460
hgdprs587777460
ensemblrs587777460
gopubmedrs587777460
geneviewrs587777460
scholarrs587777460
googlers587777460
pharmgkbrs587777460
gwascentralrs587777460
openSNPrs587777460
23andMers587777460
23andMe allrs587777460
SNP Nexus

SNPshotrs587777460
SNPdbers587777460
MSV3drs587777460
GWAS Ctlgrs587777460
Max Magnitude0
ClinVar
Risk rs587777460(A;A)
Alt rs587777460(A;A)
Reference rs587777460(G;G)
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.11141556G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128402.3,