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rs1060501105

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501105(A;T)
Make rs1060501105(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position102615266
GeneSUFU
is asnp
is mentioned by
dbSNPrs1060501105
dbSNP (old)rs1060501105
ClinGenrs1060501105
ebirs1060501105
HLIrs1060501105
Exacrs1060501105
Gnomadrs1060501105
Varsomers1060501105
Maprs1060501105
PheGenIrs1060501105
Biobankrs1060501105
1000 genomesrs1060501105
hgdprs1060501105
ensemblrs1060501105
gopubmedrs1060501105
geneviewrs1060501105
scholarrs1060501105
googlers1060501105
pharmgkbrs1060501105
gwascentralrs1060501105
openSNPrs1060501105
23andMers1060501105
23andMe allrs1060501105
SNPshotrs1060501105
SNPdbers1060501105
MSV3drs1060501105
GWAS Ctlgrs1060501105
Max Magnitude0
ClinVar
Risk rs1060501105(T;T)
Alt rs1060501105(T;T)
Reference Rs1060501105(A;A)
Significance Probable-Pathogenic
Disease Gorlin syndrome Medulloblastoma
Variation info
Gene SUFU
CLNDBN Gorlin syndrome Medulloblastoma
Reversed 0
HGVS NC_000010.10:g.104375023A>T
CLNSRC
CLNACC RCV000472343.1,