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rs878854193

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854193(G;T)
Make rs878854193(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45332573
GeneMUTYH
is asnp
is mentioned by
dbSNPrs878854193
ebirs878854193
HLIrs878854193
Exacrs878854193
Varsomers878854193
Maprs878854193
PheGenIrs878854193
hapmaprs878854193
1000 genomesrs878854193
hgdprs878854193
ensemblrs878854193
gopubmedrs878854193
geneviewrs878854193
scholarrs878854193
googlers878854193
pharmgkbrs878854193
gwascentralrs878854193
openSNPrs878854193
23andMers878854193
23andMe allrs878854193
SNP Nexus

SNPshotrs878854193
SNPdbers878854193
MSV3drs878854193
GWAS Ctlgrs878854193
Max Magnitude0
ClinVar
Risk rs878854193(T;T)
Alt rs878854193(T;T)
Reference rs878854193(G;G)
Significance Probable-Pathogenic
Disease MYH-associated polyposis
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis
Reversed 1
HGVS NC_000001.10:g.45798245C>A
CLNSRC
CLNACC RCV000230698.1,