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rs63751059

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751059(-;-)
Make rs63751059(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429914
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751059
ebirs63751059
HLIrs63751059
Exacrs63751059
Varsomers63751059
Maprs63751059
PheGenIrs63751059
hapmaprs63751059
1000 genomesrs63751059
hgdprs63751059
ensemblrs63751059
gopubmedrs63751059
geneviewrs63751059
scholarrs63751059
googlers63751059
pharmgkbrs63751059
gwascentralrs63751059
openSNPrs63751059
23andMers63751059
23andMe allrs63751059
SNP Nexus

SNPshotrs63751059
SNPdbers63751059
MSV3drs63751059
GWAS Ctlgrs63751059
Max Magnitude0
ClinVar
Risk rs63751059(;)
Alt rs63751059(;)
Reference rs63751059(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657053delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076078.2,