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rs63751027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751027(A;A)
Make rs63751027(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47416387
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751027
ClinGenrs63751027
ebirs63751027
HLIrs63751027
Exacrs63751027
Varsomers63751027
Maprs63751027
PheGenIrs63751027
hapmaprs63751027
1000 genomesrs63751027
hgdprs63751027
ensemblrs63751027
gopubmedrs63751027
geneviewrs63751027
scholarrs63751027
googlers63751027
pharmgkbrs63751027
gwascentralrs63751027
openSNPrs63751027
23andMers63751027
23andMe allrs63751027
SNP Nexus

SNPshotrs63751027
SNPdbers63751027
MSV3drs63751027
GWAS Ctlgrs63751027
Max Magnitude0
ClinVar
Risk rs63751027(A;A)
Alt rs63751027(A;A)
Reference Rs63751027(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643526G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076004.2,