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rs878854603

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854603(-;-)
Make rs878854603(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position40635947
GeneSMARCE1
is asnp
is mentioned by
dbSNPrs878854603
ebirs878854603
HLIrs878854603
Exacrs878854603
Varsomers878854603
Maprs878854603
PheGenIrs878854603
hapmaprs878854603
1000 genomesrs878854603
hgdprs878854603
ensemblrs878854603
gopubmedrs878854603
geneviewrs878854603
scholarrs878854603
googlers878854603
pharmgkbrs878854603
gwascentralrs878854603
openSNPrs878854603
23andMers878854603
23andMe allrs878854603
SNP Nexus

SNPshotrs878854603
SNPdbers878854603
MSV3drs878854603
GWAS Ctlgrs878854603
Max Magnitude0
ClinVar
Risk rs878854603(;)
Alt rs878854603(;)
Reference rs878854603(T;T)
Significance Pathogenic
Disease Meningioma
Variation info
Gene SMARCE1
CLNDBN Meningioma, familial
Reversed 1
HGVS NC_000017.10:g.38792199delA
CLNSRC
CLNACC RCV000231727.1,