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rs529008617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs529008617(A;A)
Make rs529008617(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position45331529
GeneMUTYH
is asnp
is mentioned by
dbSNPrs529008617
ebirs529008617
HLIrs529008617
Exacrs529008617
Varsomers529008617
Maprs529008617
PheGenIrs529008617
hapmaprs529008617
1000 genomesrs529008617
hgdprs529008617
ensemblrs529008617
gopubmedrs529008617
geneviewrs529008617
scholarrs529008617
googlers529008617
pharmgkbrs529008617
gwascentralrs529008617
openSNPrs529008617
23andMers529008617
23andMe allrs529008617
SNP Nexus

SNPshotrs529008617
SNPdbers529008617
MSV3drs529008617
GWAS Ctlgrs529008617
Max Magnitude0
ClinVar
Risk rs529008617(A;A)
Alt rs529008617(A;A)
Reference rs529008617(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Carcinoma of colon MYH-associated polyposis
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome Carcinoma of colon MYH-associated polyposis
Reversed 0
HGVS NC_000001.10:g.45797201G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000131914.2, RCV000144633.1, RCV000191934.1,