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rs63751007

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751007(-;-)
Make rs63751007(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47482806
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751007
ebirs63751007
HLIrs63751007
Exacrs63751007
Varsomers63751007
Maprs63751007
PheGenIrs63751007
hapmaprs63751007
1000 genomesrs63751007
hgdprs63751007
ensemblrs63751007
gopubmedrs63751007
geneviewrs63751007
scholarrs63751007
googlers63751007
pharmgkbrs63751007
gwascentralrs63751007
openSNPrs63751007
23andMers63751007
23andMe allrs63751007
SNP Nexus

SNPshotrs63751007
SNPdbers63751007
MSV3drs63751007
GWAS Ctlgrs63751007
Max Magnitude0
ClinVar
Risk rs63751007(;)
Alt rs63751007(;)
Reference rs63751007(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47709945delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076537.2,