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rs1060501395

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501395(C;T)
Make rs1060501395(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position40636451
GeneSMARCE1
is asnp
is mentioned by
dbSNPrs1060501395
dbSNP (old)rs1060501395
ClinGenrs1060501395
ebirs1060501395
HLIrs1060501395
Exacrs1060501395
Gnomadrs1060501395
Varsomers1060501395
Maprs1060501395
PheGenIrs1060501395
Biobankrs1060501395
1000 genomesrs1060501395
hgdprs1060501395
ensemblrs1060501395
gopubmedrs1060501395
geneviewrs1060501395
scholarrs1060501395
googlers1060501395
pharmgkbrs1060501395
gwascentralrs1060501395
openSNPrs1060501395
23andMers1060501395
23andMe allrs1060501395
SNPshotrs1060501395
SNPdbers1060501395
MSV3drs1060501395
GWAS Ctlgrs1060501395
Max Magnitude0
ClinVar
Risk rs1060501395(T;T)
Alt rs1060501395(T;T)
Reference Rs1060501395(C;C)
Significance Pathogenic
Disease Meningioma
Variation info
Gene SMARCE1
CLNDBN Meningioma, familial
Reversed 1
HGVS NC_000017.10:g.38792703G>A
CLNSRC
CLNACC RCV000466082.1,