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rs63751413

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751413(-;-)
Make rs63751413(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429869
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751413
ebirs63751413
HLIrs63751413
Exacrs63751413
Varsomers63751413
Maprs63751413
PheGenIrs63751413
hapmaprs63751413
1000 genomesrs63751413
hgdprs63751413
ensemblrs63751413
gopubmedrs63751413
geneviewrs63751413
scholarrs63751413
googlers63751413
pharmgkbrs63751413
gwascentralrs63751413
openSNPrs63751413
23andMers63751413
23andMe allrs63751413
SNP Nexus

SNPshotrs63751413
SNPdbers63751413
MSV3drs63751413
GWAS Ctlgrs63751413
Max Magnitude0
ClinVar
Risk rs63751413(;)
Alt rs63751413(;)
Reference rs63751413(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657008delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076062.2,