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

rs587777464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777464(A;A)
Make rs587777464(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position11027807
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs587777464
ebirs587777464
HLIrs587777464
Exacrs587777464
Varsomers587777464
Maprs587777464
PheGenIrs587777464
hapmaprs587777464
1000 genomesrs587777464
hgdprs587777464
ensemblrs587777464
gopubmedrs587777464
geneviewrs587777464
scholarrs587777464
googlers587777464
pharmgkbrs587777464
gwascentralrs587777464
openSNPrs587777464
23andMers587777464
23andMe allrs587777464
SNP Nexus

SNPshotrs587777464
SNPdbers587777464
MSV3drs587777464
GWAS Ctlgrs587777464
Max Magnitude0
ClinVar
Risk rs587777464(A;A)
Alt rs587777464(A;A)
Reference rs587777464(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.11138483G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128406.3,