Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751159

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751159(-;-)
Make rs63751159(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414312
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751159
ebirs63751159
HLIrs63751159
Exacrs63751159
Varsomers63751159
Maprs63751159
PheGenIrs63751159
hapmaprs63751159
1000 genomesrs63751159
hgdprs63751159
ensemblrs63751159
gopubmedrs63751159
geneviewrs63751159
scholarrs63751159
googlers63751159
pharmgkbrs63751159
gwascentralrs63751159
openSNPrs63751159
23andMers63751159
23andMe allrs63751159
SNP Nexus

SNPshotrs63751159
SNPdbers63751159
MSV3drs63751159
GWAS Ctlgrs63751159
Max Magnitude0
ClinVar
Risk rs63751159(;)
Alt rs63751159(;)
Reference rs63751159(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641451delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076732.2,