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rs63751483

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751483(-;-)
Make rs63751483(-;TT)
Make rs63751483(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47416391
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751483
ebirs63751483
HLIrs63751483
Exacrs63751483
Varsomers63751483
Maprs63751483
PheGenIrs63751483
hapmaprs63751483
1000 genomesrs63751483
hgdprs63751483
ensemblrs63751483
gopubmedrs63751483
geneviewrs63751483
scholarrs63751483
googlers63751483
pharmgkbrs63751483
gwascentralrs63751483
openSNPrs63751483
23andMers63751483
23andMe allrs63751483
SNP Nexus

SNPshotrs63751483
SNPdbers63751483
MSV3drs63751483
GWAS Ctlgrs63751483
Max Magnitude0
ClinVar
Risk rs63751483(TT;TT)
Alt rs63751483(TT;TT)
Reference rs63751483(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643529_47643530dupTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076006.2,