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rs1057517765

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517765(A;G)
Make rs1057517765(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position45332466
GeneMUTYH
is asnp
is mentioned by
dbSNPrs1057517765
dbSNP (old)rs1057517765
ClinGenrs1057517765
ebirs1057517765
HLIrs1057517765
Exacrs1057517765
Gnomadrs1057517765
Varsomers1057517765
Maprs1057517765
PheGenIrs1057517765
Biobankrs1057517765
1000 genomesrs1057517765
hgdprs1057517765
ensemblrs1057517765
gopubmedrs1057517765
geneviewrs1057517765
scholarrs1057517765
googlers1057517765
pharmgkbrs1057517765
gwascentralrs1057517765
openSNPrs1057517765
23andMers1057517765
23andMe allrs1057517765
SNPshotrs1057517765
SNPdbers1057517765
MSV3drs1057517765
GWAS Ctlgrs1057517765
Max Magnitude0
ClinVar
Risk rs1057517765(C;C) rs1057517765(G;G)
Alt rs1057517765(C;C) rs1057517765(G;G)
Reference Rs1057517765(A;A)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene MUTYH
CLNDBN not provided not specified
Reversed 1
HGVS NC_000001.10:g.45798138T>C; NC_000001.10:g.45798138T>G
CLNSRC
CLNACC RCV000414648.1, RCV000479523.1,