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rs63751290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751290(-;-)
Make rs63751290(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410126
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751290
ebirs63751290
HLIrs63751290
Exacrs63751290
Varsomers63751290
Maprs63751290
PheGenIrs63751290
hapmaprs63751290
1000 genomesrs63751290
hgdprs63751290
ensemblrs63751290
gopubmedrs63751290
geneviewrs63751290
scholarrs63751290
googlers63751290
pharmgkbrs63751290
gwascentralrs63751290
openSNPrs63751290
23andMers63751290
23andMe allrs63751290
SNP Nexus

SNPshotrs63751290
SNPdbers63751290
MSV3drs63751290
GWAS Ctlgrs63751290
Max Magnitude0
ClinVar
Risk rs63751290(;)
Alt rs63751290(;)
Reference rs63751290(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637265delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076595.2,