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rs1057520660

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520660(A;A)
Make rs1057520660(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position45332960
GeneMUTYH
is asnp
is mentioned by
dbSNPrs1057520660
dbSNP (classic)rs1057520660
ClinGenrs1057520660
ebirs1057520660
HLIrs1057520660
Exacrs1057520660
Gnomadrs1057520660
Varsomers1057520660
LitVarrs1057520660
Maprs1057520660
PheGenIrs1057520660
Biobankrs1057520660
1000 genomesrs1057520660
hgdprs1057520660
ensemblrs1057520660
geneviewrs1057520660
scholarrs1057520660
googlers1057520660
pharmgkbrs1057520660
gwascentralrs1057520660
openSNPrs1057520660
23andMers1057520660
SNPshotrs1057520660
SNPdbers1057520660
MSV3drs1057520660
GWAS Ctlgrs1057520660
Max Magnitude0
ClinVar
Risk rs1057520660(A;A) rs1057520660(C;C)
Alt rs1057520660(A;A) rs1057520660(C;C)
Reference Rs1057520660(G;G)
Significance Pathogenic
Disease MYH-associated polyposis not provided
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis not provided
Reversed 1
HGVS NC_000001.10:g.45798632C>G; NC_000001.10:g.45798632C>T
CLNSRC
CLNACC RCV000463536.1, RCV000417586.1,