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rs1060501109

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501109(C;T)
Make rs1060501109(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position102550088
GeneSUFU
is asnp
is mentioned by
dbSNPrs1060501109
dbSNP (old)rs1060501109
ClinGenrs1060501109
ebirs1060501109
HLIrs1060501109
Exacrs1060501109
Gnomadrs1060501109
Varsomers1060501109
Maprs1060501109
PheGenIrs1060501109
Biobankrs1060501109
1000 genomesrs1060501109
hgdprs1060501109
ensemblrs1060501109
gopubmedrs1060501109
geneviewrs1060501109
scholarrs1060501109
googlers1060501109
pharmgkbrs1060501109
gwascentralrs1060501109
openSNPrs1060501109
23andMers1060501109
23andMe allrs1060501109
SNPshotrs1060501109
SNPdbers1060501109
MSV3drs1060501109
GWAS Ctlgrs1060501109
Max Magnitude0
ClinVar
Risk rs1060501109(T;T)
Alt rs1060501109(T;T)
Reference Rs1060501109(C;C)
Significance Pathogenic
Disease Gorlin syndrome Medulloblastoma
Variation info
Gene SUFU
CLNDBN Gorlin syndrome Medulloblastoma
Reversed 0
HGVS NC_000010.10:g.104309845C>T
CLNSRC
CLNACC RCV000460887.1,