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rs200495564

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200495564(A;A)
Make rs200495564(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position45332446
GeneMUTYH
is asnp
is mentioned by
dbSNPrs200495564
ebirs200495564
HLIrs200495564
Exacrs200495564
Varsomers200495564
Maprs200495564
PheGenIrs200495564
hapmaprs200495564
1000 genomesrs200495564
hgdprs200495564
ensemblrs200495564
gopubmedrs200495564
geneviewrs200495564
scholarrs200495564
googlers200495564
pharmgkbrs200495564
gwascentralrs200495564
openSNPrs200495564
23andMers200495564
23andMe allrs200495564
SNP Nexus

SNPshotrs200495564
SNPdbers200495564
MSV3drs200495564
GWAS Ctlgrs200495564
Max Magnitude0
ClinVar
Risk rs200495564(A;A)
Alt rs200495564(A;A)
Reference rs200495564(G;G)
Significance Other
Disease MYH-associated polyposis Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.45798118G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000034678.2, RCV000129829.2,