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rs863224502

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 3 Carrier of a MUTYH-related familial adenomatous polyposis mutation
Make rs863224502(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45331184
GeneMUTYH
is asnp
is mentioned by
dbSNPrs863224502
dbSNP (classic)rs863224502
ClinGenrs863224502
ebirs863224502
HLIrs863224502
Exacrs863224502
Gnomadrs863224502
Varsomers863224502
LitVarrs863224502
Maprs863224502
PheGenIrs863224502
Biobankrs863224502
1000 genomesrs863224502
hgdprs863224502
ensemblrs863224502
geneviewrs863224502
scholarrs863224502
googlers863224502
pharmgkbrs863224502
gwascentralrs863224502
openSNPrs863224502
23andMers863224502
SNPshotrs863224502
SNPdbers863224502
MSV3drs863224502
GWAS Ctlgrs863224502
Max Magnitude3
ClinVar
Risk rs863224502(T;T)
Alt rs863224502(T;T)
Reference Rs863224502(A;A)
Significance Pathogenic
Disease MYH-associated polyposis
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis
Reversed 1
HGVS NC_000001.10:g.45796856T>A
CLNSRC
CLNACC RCV000198593.1,