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rs372267274

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372267274(C;T)
Make rs372267274(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45333171
GeneMUTYH
is asnp
is mentioned by
dbSNPrs372267274
ebirs372267274
HLIrs372267274
Exacrs372267274
Varsomers372267274
Maprs372267274
PheGenIrs372267274
hapmaprs372267274
1000 genomesrs372267274
hgdprs372267274
ensemblrs372267274
gopubmedrs372267274
geneviewrs372267274
scholarrs372267274
googlers372267274
pharmgkbrs372267274
gwascentralrs372267274
openSNPrs372267274
23andMers372267274
23andMe allrs372267274
SNP Nexus

SNPshotrs372267274
SNPdbers372267274
MSV3drs372267274
GWAS Ctlgrs372267274
Max Magnitude0
ClinVar
Risk rs372267274(T;T)
Alt rs372267274(T;T)
Reference rs372267274(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations MYH-associated polyposis Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Tumor susceptibility linked to germline BAP1 mutations MYH-associated polyposis Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.45798843C>G; NC_000001.10:g.45798843C>T
CLNSRC
CLNACC RCV000221410.1, RCV000230931.1, RCV000166470.1,