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rs376790729

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376790729(C;T)
Make rs376790729(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45331223
GeneMUTYH
is asnp
is mentioned by
dbSNPrs376790729
ebirs376790729
HLIrs376790729
Exacrs376790729
Varsomers376790729
Maprs376790729
PheGenIrs376790729
hapmaprs376790729
1000 genomesrs376790729
hgdprs376790729
ensemblrs376790729
gopubmedrs376790729
geneviewrs376790729
scholarrs376790729
googlers376790729
pharmgkbrs376790729
gwascentralrs376790729
openSNPrs376790729
23andMers376790729
23andMe allrs376790729
SNP Nexus

SNPshotrs376790729
SNPdbers376790729
MSV3drs376790729
GWAS Ctlgrs376790729
Max Magnitude0
ClinVar
Risk rs376790729(A,T;A,T)
Alt rs376790729(A,T;A,T)
Reference rs376790729(C;C)
Significance Pathogenic
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.45796895C>A; NC_000001.10:g.45796895C>T
CLNSRC
CLNACC RCV000234544.1, RCV000165664.1, RCV000200800.2,