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rs786203161

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203161(A;C)
Make rs786203161(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45332836
GeneMUTYH
is asnp
is mentioned by
dbSNPrs786203161
ebirs786203161
HLIrs786203161
Exacrs786203161
Varsomers786203161
Maprs786203161
PheGenIrs786203161
hapmaprs786203161
1000 genomesrs786203161
hgdprs786203161
ensemblrs786203161
gopubmedrs786203161
geneviewrs786203161
scholarrs786203161
googlers786203161
pharmgkbrs786203161
gwascentralrs786203161
openSNPrs786203161
23andMers786203161
23andMe allrs786203161
SNP Nexus

SNPshotrs786203161
SNPdbers786203161
MSV3drs786203161
GWAS Ctlgrs786203161
Max Magnitude0
ClinVar
Risk rs786203161(C;C)
Alt rs786203161(C;C)
Reference rs786203161(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45798508T>G
CLNSRC
CLNACC RCV000166350.1,