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rs797045990

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGAG;TGAG) 0 common in clinvar
Make rs797045990(-;-)
Make rs797045990(-;TGAG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position40632282
GeneSMARCE1
is asnp
is mentioned by
dbSNPrs797045990
dbSNP (old)rs797045990
ClinGenrs797045990
ebirs797045990
HLIrs797045990
Exacrs797045990
Varsomers797045990
Maprs797045990
PheGenIrs797045990
Biobankrs797045990
1000 genomesrs797045990
hgdprs797045990
ensemblrs797045990
gopubmedrs797045990
geneviewrs797045990
scholarrs797045990
googlers797045990
pharmgkbrs797045990
gwascentralrs797045990
openSNPrs797045990
23andMers797045990
23andMe allrs797045990
SNP Nexus

SNPshotrs797045990
SNPdbers797045990
MSV3drs797045990
GWAS Ctlgrs797045990
Max Magnitude0
ClinVar
Risk rs797045990(-;-)
Alt rs797045990(-;-)
Reference Rs797045990(TGAG;TGAG)
Significance Pathogenic
Disease Meningioma
Variation info
Gene SMARCE1
CLNDBN Meningioma, familial
Reversed 1
HGVS NC_000017.10:g.38788534_38788537delCTCA
CLNSRC
CLNACC RCV000194068.1,