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rs730881832

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881832(A;A)
Make rs730881832(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45333168
GeneMUTYH
is asnp
is mentioned by
dbSNPrs730881832
ebirs730881832
HLIrs730881832
Exacrs730881832
Varsomers730881832
Maprs730881832
PheGenIrs730881832
hapmaprs730881832
1000 genomesrs730881832
hgdprs730881832
ensemblrs730881832
gopubmedrs730881832
geneviewrs730881832
scholarrs730881832
googlers730881832
pharmgkbrs730881832
gwascentralrs730881832
openSNPrs730881832
23andMers730881832
23andMe allrs730881832
SNP Nexus

SNPshotrs730881832
SNPdbers730881832
MSV3drs730881832
GWAS Ctlgrs730881832
Max Magnitude0
ClinVar
Risk rs730881832(A;A)
Alt rs730881832(A;A)
Reference rs730881832(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000001.10:g.45798840A>T
CLNSRC
CLNACC RCV000160751.3, RCV000212700.1,