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rs587777462

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777462(C;T)
Make rs587777462(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position10986476
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs587777462
ebirs587777462
HLIrs587777462
Exacrs587777462
Varsomers587777462
Maprs587777462
PheGenIrs587777462
hapmaprs587777462
1000 genomesrs587777462
hgdprs587777462
ensemblrs587777462
gopubmedrs587777462
geneviewrs587777462
scholarrs587777462
googlers587777462
pharmgkbrs587777462
gwascentralrs587777462
openSNPrs587777462
23andMers587777462
23andMe allrs587777462
SNP Nexus

SNPshotrs587777462
SNPdbers587777462
MSV3drs587777462
GWAS Ctlgrs587777462
Max Magnitude0
ClinVar
Risk rs587777462(T;T)
Alt rs587777462(T;T)
Reference rs587777462(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.11097152C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000128404.3,