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rs1060503015

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503015(C;T)
Make rs1060503015(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position23791780
GeneSMARCB1
is asnp
is mentioned by
dbSNPrs1060503015
dbSNP (old)rs1060503015
ClinGenrs1060503015
ebirs1060503015
HLIrs1060503015
Exacrs1060503015
Gnomadrs1060503015
Varsomers1060503015
LitVarrs1060503015
Maprs1060503015
PheGenIrs1060503015
Biobankrs1060503015
1000 genomesrs1060503015
hgdprs1060503015
ensemblrs1060503015
gopubmedrs1060503015
geneviewrs1060503015
scholarrs1060503015
googlers1060503015
pharmgkbrs1060503015
gwascentralrs1060503015
openSNPrs1060503015
23andMers1060503015
23andMe allrs1060503015
SNPshotrs1060503015
SNPdbers1060503015
MSV3drs1060503015
GWAS Ctlgrs1060503015
Max Magnitude0
ClinVar
Risk rs1060503015(T;T)
Alt rs1060503015(T;T)
Reference Rs1060503015(C;C)
Significance Pathogenic
Disease Rhabdoid tumor predisposition syndrome 1 Schwannomatosis
Variation info
Gene SMARCB1
CLNDBN Rhabdoid tumor predisposition syndrome 1 Schwannomatosis
Reversed 0
HGVS NC_000022.10:g.24133967C>T
CLNSRC
CLNACC RCV000467994.1,