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rs63749872

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs63749872(-;-)
Make rs63749872(-;TT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408467
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749872
ebirs63749872
HLIrs63749872
Exacrs63749872
Varsomers63749872
Maprs63749872
PheGenIrs63749872
hapmaprs63749872
1000 genomesrs63749872
hgdprs63749872
ensemblrs63749872
gopubmedrs63749872
geneviewrs63749872
scholarrs63749872
googlers63749872
pharmgkbrs63749872
gwascentralrs63749872
openSNPrs63749872
23andMers63749872
23andMe allrs63749872
SNP Nexus

SNPshotrs63749872
SNPdbers63749872
MSV3drs63749872
GWAS Ctlgrs63749872
Max Magnitude0
ClinVar
Risk rs63749872(;)
Alt rs63749872(;)
Reference rs63749872(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635606_47635607delTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076548.2,