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rs1057520735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520735(C;G)
Make rs1057520735(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47476388
GeneMSH2
is asnp
is mentioned by
dbSNPrs1057520735
dbSNP (old)rs1057520735
ClinGenrs1057520735
ebirs1057520735
HLIrs1057520735
Exacrs1057520735
Gnomadrs1057520735
Varsomers1057520735
LitVarrs1057520735
Maprs1057520735
PheGenIrs1057520735
Biobankrs1057520735
1000 genomesrs1057520735
hgdprs1057520735
ensemblrs1057520735
gopubmedrs1057520735
geneviewrs1057520735
scholarrs1057520735
googlers1057520735
pharmgkbrs1057520735
gwascentralrs1057520735
openSNPrs1057520735
23andMers1057520735
23andMe allrs1057520735
SNPshotrs1057520735
SNPdbers1057520735
MSV3drs1057520735
GWAS Ctlgrs1057520735
Max Magnitude0
ClinVar
Risk rs1057520735(G;G)
Alt rs1057520735(G;G)
Reference Rs1057520735(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47703527C>G
CLNSRC
CLNACC RCV000438851.1,