Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776578(A;A)
Make rs587776578(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position102599545
GeneSUFU
is asnp
is mentioned by
dbSNPrs587776578
ebirs587776578
HLIrs587776578
Exacrs587776578
Varsomers587776578
Maprs587776578
PheGenIrs587776578
hapmaprs587776578
1000 genomesrs587776578
hgdprs587776578
ensemblrs587776578
gopubmedrs587776578
geneviewrs587776578
scholarrs587776578
googlers587776578
pharmgkbrs587776578
gwascentralrs587776578
openSNPrs587776578
23andMers587776578
23andMe allrs587776578
SNP Nexus

SNPshotrs587776578
SNPdbers587776578
MSV3drs587776578
GWAS Ctlgrs587776578
Max Magnitude0
ClinVar
Risk rs587776578(A,C;A,C)
Alt rs587776578(A,C;A,C)
Reference rs587776578(G;G)
Significance Pathogenic
Disease Medulloblastoma Gorlin syndrome
Variation info
Gene SUFU
CLNDBN Medulloblastoma, desmoplastic Gorlin syndrome
Reversed 0
HGVS NC_000010.10:g.104359302G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003752.4, RCV000003753.2,