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rs374950566

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374950566(A;A)
Make rs374950566(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45332215
GeneMUTYH
is asnp
is mentioned by
dbSNPrs374950566
ebirs374950566
HLIrs374950566
Exacrs374950566
Varsomers374950566
Maprs374950566
PheGenIrs374950566
hapmaprs374950566
1000 genomesrs374950566
hgdprs374950566
ensemblrs374950566
gopubmedrs374950566
geneviewrs374950566
scholarrs374950566
googlers374950566
pharmgkbrs374950566
gwascentralrs374950566
openSNPrs374950566
23andMers374950566
23andMe allrs374950566
SNP Nexus

SNPshotrs374950566
SNPdbers374950566
MSV3drs374950566
GWAS Ctlgrs374950566
Max Magnitude0
ClinVar
Risk rs374950566(A;A)
Alt rs374950566(A;A)
Reference rs374950566(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000001.10:g.45797887G>A
CLNSRC
CLNACC RCV000164625.1, RCV000235921.1,