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rs63749878

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63749878(-;-)
Make rs63749878(-;A)
Make rs63749878(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476432
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749878
ebirs63749878
HLIrs63749878
Exacrs63749878
Varsomers63749878
Maprs63749878
PheGenIrs63749878
hapmaprs63749878
1000 genomesrs63749878
hgdprs63749878
ensemblrs63749878
gopubmedrs63749878
geneviewrs63749878
scholarrs63749878
googlers63749878
pharmgkbrs63749878
gwascentralrs63749878
openSNPrs63749878
23andMers63749878
23andMe allrs63749878
SNP Nexus

SNPshotrs63749878
SNPdbers63749878
MSV3drs63749878
GWAS Ctlgrs63749878
Max Magnitude0
ClinVar
Risk rs63749878(A;A)
Alt rs63749878(A;A)
Reference rs63749878(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703571dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076379.2,