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rs63749850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(D;D) 0
Make rs63749850(-;-)
Make rs63749850(-;CA)
Make rs63749850(CA;CA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429862
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749850
ebirs63749850
HLIrs63749850
Exacrs63749850
Varsomers63749850
Maprs63749850
PheGenIrs63749850
hapmaprs63749850
1000 genomesrs63749850
hgdprs63749850
ensemblrs63749850
gopubmedrs63749850
geneviewrs63749850
scholarrs63749850
googlers63749850
pharmgkbrs63749850
gwascentralrs63749850
openSNPrs63749850
23andMers63749850
23andMe allrs63749850
SNP Nexus

SNPshotrs63749850
SNPdbers63749850
MSV3drs63749850
GWAS Ctlgrs63749850
Max Magnitude0
ClinVar
Risk rs63749850(CA;CA)
Alt rs63749850(CA;CA)
Reference rs63749850(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657000_47657001dupCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076058.2,