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rs63749852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63749852(-;-)
Make rs63749852(-;A)
Make rs63749852(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47416311
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749852
ebirs63749852
HLIrs63749852
Exacrs63749852
Varsomers63749852
Maprs63749852
PheGenIrs63749852
hapmaprs63749852
1000 genomesrs63749852
hgdprs63749852
ensemblrs63749852
gopubmedrs63749852
geneviewrs63749852
scholarrs63749852
googlers63749852
pharmgkbrs63749852
gwascentralrs63749852
openSNPrs63749852
23andMers63749852
23andMe allrs63749852
SNP Nexus

SNPshotrs63749852
SNPdbers63749852
MSV3drs63749852
GWAS Ctlgrs63749852
Max Magnitude0
ClinVar
Risk rs63749852(A;A)
Alt rs63749852(A;A)
Reference rs63749852(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643450dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076763.2,