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rs63751155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751155(A;A)
Make rs63751155(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478289
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751155
ebirs63751155
HLIrs63751155
Exacrs63751155
Varsomers63751155
Maprs63751155
PheGenIrs63751155
hapmaprs63751155
1000 genomesrs63751155
hgdprs63751155
ensemblrs63751155
gopubmedrs63751155
geneviewrs63751155
scholarrs63751155
googlers63751155
pharmgkbrs63751155
gwascentralrs63751155
openSNPrs63751155
23andMers63751155
23andMe allrs63751155
SNP Nexus

SNPshotrs63751155
SNPdbers63751155
MSV3drs63751155
GWAS Ctlgrs63751155
Max Magnitude0
ClinVar
Risk rs63751155(A,G;A,G)
Alt rs63751155(A,G;A,G)
Reference rs63751155(C;C)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47705428C>A; NC_000002.11:g.47705428C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076434.2, RCV000236386.1, RCV000076435.2,