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rs193922375

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs193922375(-;-)
Make rs193922375(-;G)
Make rs193922375(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414336
GeneMSH2
is asnp
is mentioned by
dbSNPrs193922375
ebirs193922375
HLIrs193922375
Exacrs193922375
Varsomers193922375
Maprs193922375
PheGenIrs193922375
hapmaprs193922375
1000 genomesrs193922375
hgdprs193922375
ensemblrs193922375
gopubmedrs193922375
geneviewrs193922375
scholarrs193922375
googlers193922375
pharmgkbrs193922375
gwascentralrs193922375
openSNPrs193922375
23andMers193922375
23andMe allrs193922375
SNP Nexus

SNPshotrs193922375
SNPdbers193922375
MSV3drs193922375
GWAS Ctlgrs193922375
Max Magnitude0
ClinVar
Risk rs193922375(G;G)
Alt rs193922375(G;G)
Reference rs193922375(;)
Significance Other
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47641475dupG
CLNSRC ClinVar LabCorp
CLNACC RCV000030255.2, RCV000162420.1,