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rs63751115

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(TT;TT) 0 common in clinvar
Make rs63751115(-;-)
Make rs63751115(-;TT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414357
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751115
ebirs63751115
HLIrs63751115
Exacrs63751115
Varsomers63751115
Maprs63751115
PheGenIrs63751115
hapmaprs63751115
1000 genomesrs63751115
hgdprs63751115
ensemblrs63751115
gopubmedrs63751115
geneviewrs63751115
scholarrs63751115
googlers63751115
pharmgkbrs63751115
gwascentralrs63751115
openSNPrs63751115
23andMers63751115
23andMe allrs63751115
SNP Nexus

SNPshotrs63751115
SNPdbers63751115
MSV3drs63751115
GWAS Ctlgrs63751115
Max Magnitude0
ClinVar
Risk rs63751115(;)
Alt rs63751115(;)
Reference rs63751115(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641496_47641497delTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076742.2,