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rs267608010

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608010(A;A)
Make rs267608010(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478520
GeneMSH2
is asnp
is mentioned by
dbSNPrs267608010
ebirs267608010
HLIrs267608010
Exacrs267608010
Varsomers267608010
Maprs267608010
PheGenIrs267608010
hapmaprs267608010
1000 genomesrs267608010
hgdprs267608010
ensemblrs267608010
gopubmedrs267608010
geneviewrs267608010
scholarrs267608010
googlers267608010
pharmgkbrs267608010
gwascentralrs267608010
openSNPrs267608010
23andMers267608010
23andMe allrs267608010
SNP Nexus

SNPshotrs267608010
SNPdbers267608010
MSV3drs267608010
GWAS Ctlgrs267608010
Max Magnitude0
ClinVar
Risk rs267608010(A;A)
Alt rs267608010(A;A)
Reference rs267608010(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705659G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076478.2,