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rs63751105

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751105(A;A)
Make rs63751105(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478353
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751105
ebirs63751105
HLIrs63751105
Exacrs63751105
Varsomers63751105
Maprs63751105
PheGenIrs63751105
hapmaprs63751105
1000 genomesrs63751105
hgdprs63751105
ensemblrs63751105
gopubmedrs63751105
geneviewrs63751105
scholarrs63751105
googlers63751105
pharmgkbrs63751105
gwascentralrs63751105
openSNPrs63751105
23andMers63751105
23andMe allrs63751105
SNP Nexus

SNPshotrs63751105
SNPdbers63751105
MSV3drs63751105
GWAS Ctlgrs63751105
Max Magnitude0
ClinVar
Risk rs63751105(A,C;A,C)
Alt rs63751105(A,C;A,C)
Reference rs63751105(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705492G>A; NC_000002.11:g.47705492G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076451.2, RCV000076452.2,