Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607985

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607985(A;G)
Make rs267607985(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475073
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607985
ebirs267607985
HLIrs267607985
Exacrs267607985
Varsomers267607985
Maprs267607985
PheGenIrs267607985
hapmaprs267607985
1000 genomesrs267607985
hgdprs267607985
ensemblrs267607985
gopubmedrs267607985
geneviewrs267607985
scholarrs267607985
googlers267607985
pharmgkbrs267607985
gwascentralrs267607985
openSNPrs267607985
23andMers267607985
23andMe allrs267607985
SNP Nexus

SNPshotrs267607985
SNPdbers267607985
MSV3drs267607985
GWAS Ctlgrs267607985
Max Magnitude0
ClinVar
Risk rs267607985(G;G)
Alt rs267607985(G;G)
Reference rs267607985(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702212A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076292.2,