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rs63751147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751147(C;C)
Make rs63751147(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47416375
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751147
ebirs63751147
HLIrs63751147
Exacrs63751147
Varsomers63751147
Maprs63751147
PheGenIrs63751147
hapmaprs63751147
1000 genomesrs63751147
hgdprs63751147
ensemblrs63751147
gopubmedrs63751147
geneviewrs63751147
scholarrs63751147
googlers63751147
pharmgkbrs63751147
gwascentralrs63751147
openSNPrs63751147
23andMers63751147
23andMe allrs63751147
SNP Nexus

SNPshotrs63751147
SNPdbers63751147
MSV3drs63751147
GWAS Ctlgrs63751147
Max Magnitude0
ClinVar
Risk rs63751147(C;C)
Alt rs63751147(C;C)
Reference rs63751147(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643514T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076002.2,