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rs63751299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751299(-;-)
Make rs63751299(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47471023
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751299
ebirs63751299
HLIrs63751299
Exacrs63751299
Varsomers63751299
Maprs63751299
PheGenIrs63751299
hapmaprs63751299
1000 genomesrs63751299
hgdprs63751299
ensemblrs63751299
gopubmedrs63751299
geneviewrs63751299
scholarrs63751299
googlers63751299
pharmgkbrs63751299
gwascentralrs63751299
openSNPrs63751299
23andMers63751299
23andMe allrs63751299
SNP Nexus

SNPshotrs63751299
SNPdbers63751299
MSV3drs63751299
GWAS Ctlgrs63751299
Max Magnitude0
ClinVar
Risk rs63751299(;)
Alt rs63751299(;)
Reference rs63751299(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698162delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076258.2,