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rs63751668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751668(A;A)
Make rs63751668(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position47475270
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751668
ebirs63751668
HLIrs63751668
Exacrs63751668
Varsomers63751668
Maprs63751668
PheGenIrs63751668
hapmaprs63751668
1000 genomesrs63751668
hgdprs63751668
ensemblrs63751668
gopubmedrs63751668
geneviewrs63751668
scholarrs63751668
googlers63751668
pharmgkbrs63751668
gwascentralrs63751668
openSNPrs63751668
23andMers63751668
23andMe allrs63751668
SNP Nexus

SNPshotrs63751668
SNPdbers63751668
MSV3drs63751668
GWAS Ctlgrs63751668
Max Magnitude0
ClinVar
Risk rs63751668(A,C;A,C)
Alt rs63751668(A,C;A,C)
Reference rs63751668(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702409G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076346.2,