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rs63751161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751161(-;-)
Make rs63751161(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476376
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751161
ebirs63751161
HLIrs63751161
Exacrs63751161
Varsomers63751161
Maprs63751161
PheGenIrs63751161
hapmaprs63751161
1000 genomesrs63751161
hgdprs63751161
ensemblrs63751161
gopubmedrs63751161
geneviewrs63751161
scholarrs63751161
googlers63751161
pharmgkbrs63751161
gwascentralrs63751161
openSNPrs63751161
23andMers63751161
23andMe allrs63751161
SNP Nexus

SNPshotrs63751161
SNPdbers63751161
MSV3drs63751161
GWAS Ctlgrs63751161
Max Magnitude0
ClinVar
Risk rs63751161(;)
Alt rs63751161(;)
Reference rs63751161(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703515delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076361.2,