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rs587776678

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776678(-;-)
Make rs587776678(-;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position23803385
GeneSMARCB1
is asnp
is mentioned by
dbSNPrs587776678
ebirs587776678
HLIrs587776678
Exacrs587776678
Varsomers587776678
Maprs587776678
PheGenIrs587776678
hapmaprs587776678
1000 genomesrs587776678
hgdprs587776678
ensemblrs587776678
gopubmedrs587776678
geneviewrs587776678
scholarrs587776678
googlers587776678
pharmgkbrs587776678
gwascentralrs587776678
openSNPrs587776678
23andMers587776678
23andMe allrs587776678
SNP Nexus

SNPshotrs587776678
SNPdbers587776678
MSV3drs587776678
GWAS Ctlgrs587776678
Max Magnitude0
ClinVar
Risk rs587776678(;)
Alt rs587776678(;)
Reference rs587776678(G;G)
Significance Pathogenic
Disease Rhabdoid tumor predisposition syndrome 1
Variation info
Gene SMARCB1
CLNDBN Rhabdoid tumor predisposition syndrome 1
Reversed 0
HGVS NC_000022.10:g.24145572delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000008488.4,