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rs587777461

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777461(A;A)
Make rs587777461(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position11035133
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs587777461
ebirs587777461
HLIrs587777461
Exacrs587777461
Varsomers587777461
Maprs587777461
PheGenIrs587777461
hapmaprs587777461
1000 genomesrs587777461
hgdprs587777461
ensemblrs587777461
gopubmedrs587777461
geneviewrs587777461
scholarrs587777461
googlers587777461
pharmgkbrs587777461
gwascentralrs587777461
openSNPrs587777461
23andMers587777461
23andMe allrs587777461
SNP Nexus

SNPshotrs587777461
SNPdbers587777461
MSV3drs587777461
GWAS Ctlgrs587777461
Max Magnitude0
ClinVar
Risk rs587777461(A;A)
Alt rs587777461(A;A)
Reference rs587777461(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.11145809G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128403.3,