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rs138775799

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138775799(A;A)
Make rs138775799(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position45333472
GeneMUTYH
is asnp
is mentioned by
dbSNPrs138775799
ebirs138775799
HLIrs138775799
Exacrs138775799
Varsomers138775799
Maprs138775799
PheGenIrs138775799
hapmaprs138775799
1000 genomesrs138775799
hgdprs138775799
ensemblrs138775799
gopubmedrs138775799
geneviewrs138775799
scholarrs138775799
googlers138775799
pharmgkbrs138775799
gwascentralrs138775799
openSNPrs138775799
23andMers138775799
23andMe allrs138775799
SNP Nexus

SNPshotrs138775799
SNPdbers138775799
MSV3drs138775799
GWAS Ctlgrs138775799
Max Magnitude0
ClinVar
Risk rs138775799(A;A)
Alt rs138775799(A;A)
Reference rs138775799(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000001.10:g.45799144G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000129018.2, RCV000235267.1,