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rs786203115

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203115(C;T)
Make rs786203115(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45332300
GeneMUTYH
is asnp
is mentioned by
dbSNPrs786203115
ebirs786203115
HLIrs786203115
Exacrs786203115
Varsomers786203115
Maprs786203115
PheGenIrs786203115
hapmaprs786203115
1000 genomesrs786203115
hgdprs786203115
ensemblrs786203115
gopubmedrs786203115
geneviewrs786203115
scholarrs786203115
googlers786203115
pharmgkbrs786203115
gwascentralrs786203115
openSNPrs786203115
23andMers786203115
23andMe allrs786203115
SNP Nexus

SNPshotrs786203115
SNPdbers786203115
MSV3drs786203115
GWAS Ctlgrs786203115
Max Magnitude0
ClinVar
Risk rs786203115(T;T)
Alt rs786203115(T;T)
Reference rs786203115(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome MYH-associated polyposis
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome MYH-associated polyposis
Reversed 1
HGVS NC_000001.10:g.45797972G>A
CLNSRC
CLNACC RCV000166279.1, RCV000198325.2,