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rs267608002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608002(A;A)
Make rs267608002(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476572
GeneMSH2
is asnp
is mentioned by
dbSNPrs267608002
ebirs267608002
HLIrs267608002
Exacrs267608002
Varsomers267608002
Maprs267608002
PheGenIrs267608002
hapmaprs267608002
1000 genomesrs267608002
hgdprs267608002
ensemblrs267608002
gopubmedrs267608002
geneviewrs267608002
scholarrs267608002
googlers267608002
pharmgkbrs267608002
gwascentralrs267608002
openSNPrs267608002
23andMers267608002
23andMe allrs267608002
SNP Nexus

SNPshotrs267608002
SNPdbers267608002
MSV3drs267608002
GWAS Ctlgrs267608002
Max Magnitude0
ClinVar
Risk rs267608002(A,C;A,C)
Alt rs267608002(A,C;A,C)
Reference rs267608002(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703711G>A; NC_000002.11:g.47703711G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076423.2, RCV000076424.2,