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rs63751142

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(I;I) 0
Make rs63751142(-;T)
Make rs63751142(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429887
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751142
dbSNP (old)rs63751142
ClinGenrs63751142
ebirs63751142
HLIrs63751142
Exacrs63751142
Varsomers63751142
Maprs63751142
PheGenIrs63751142
Biobankrs63751142
1000 genomesrs63751142
hgdprs63751142
ensemblrs63751142
gopubmedrs63751142
geneviewrs63751142
scholarrs63751142
googlers63751142
pharmgkbrs63751142
gwascentralrs63751142
openSNPrs63751142
23andMers63751142
23andMe allrs63751142
SNP Nexus

SNPshotrs63751142
SNPdbers63751142
MSV3drs63751142
GWAS Ctlgrs63751142
Max Magnitude0
ClinVar
Risk rs63751142(T;T)
Alt rs63751142(T;T)
Reference Rs63751142(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47657026dup; NC_000002.11:g.47657026dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000491975.1, RCV000076069.2, RCV000479156.1,