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rs1060501333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060501333(G;G)
Make rs1060501333(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position45332164
GeneMUTYH
is asnp
is mentioned by
dbSNPrs1060501333
dbSNP (old)rs1060501333
ClinGenrs1060501333
ebirs1060501333
HLIrs1060501333
Exacrs1060501333
Gnomadrs1060501333
Varsomers1060501333
Maprs1060501333
PheGenIrs1060501333
Biobankrs1060501333
1000 genomesrs1060501333
hgdprs1060501333
ensemblrs1060501333
gopubmedrs1060501333
geneviewrs1060501333
scholarrs1060501333
googlers1060501333
pharmgkbrs1060501333
gwascentralrs1060501333
openSNPrs1060501333
23andMers1060501333
23andMe allrs1060501333
SNPshotrs1060501333
SNPdbers1060501333
MSV3drs1060501333
GWAS Ctlgrs1060501333
Max Magnitude0
ClinVar
Risk rs1060501333(G;G)
Alt rs1060501333(G;G)
Reference Rs1060501333(T;T)
Significance Probable-Pathogenic
Disease MYH-associated polyposis
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis
Reversed 1
HGVS NC_000001.10:g.45797836A>C
CLNSRC
CLNACC RCV000469962.1,