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rs748170941

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748170941(C;T)
Make rs748170941(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45333452
GeneMUTYH
is asnp
is mentioned by
dbSNPrs748170941
ebirs748170941
HLIrs748170941
Exacrs748170941
Varsomers748170941
Maprs748170941
PheGenIrs748170941
hapmaprs748170941
1000 genomesrs748170941
hgdprs748170941
ensemblrs748170941
gopubmedrs748170941
geneviewrs748170941
scholarrs748170941
googlers748170941
pharmgkbrs748170941
gwascentralrs748170941
openSNPrs748170941
23andMers748170941
23andMe allrs748170941
SNP Nexus

SNPshotrs748170941
SNPdbers748170941
MSV3drs748170941
GWAS Ctlgrs748170941
Max Magnitude0
ClinVar
Risk rs748170941(T;T)
Alt rs748170941(T;T)
Reference rs748170941(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome MYH-associated polyposis
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome MYH-associated polyposis
Reversed 0
HGVS NC_000001.10:g.45799124C>T
CLNSRC
CLNACC RCV000164326.1, RCV000196257.1,