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rs193922374

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922374(A;G)
Make rs193922374(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410148
GeneMSH2
is asnp
is mentioned by
dbSNPrs193922374
ebirs193922374
HLIrs193922374
Exacrs193922374
Varsomers193922374
Maprs193922374
PheGenIrs193922374
hapmaprs193922374
1000 genomesrs193922374
hgdprs193922374
ensemblrs193922374
gopubmedrs193922374
geneviewrs193922374
scholarrs193922374
googlers193922374
pharmgkbrs193922374
gwascentralrs193922374
openSNPrs193922374
23andMers193922374
23andMe allrs193922374
SNP Nexus

SNPshotrs193922374
SNPdbers193922374
MSV3drs193922374
GWAS Ctlgrs193922374
Max Magnitude0
ClinVar
Risk rs193922374(G;G)
Alt rs193922374(G;G)
Reference rs193922374(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000002.11:g.47637287A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000030254.3, RCV000115531.5, RCV000212584.1,