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

rs63751129

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751129(-;-)
Make rs63751129(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475074
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751129
ebirs63751129
HLIrs63751129
Exacrs63751129
Varsomers63751129
Maprs63751129
PheGenIrs63751129
hapmaprs63751129
1000 genomesrs63751129
hgdprs63751129
ensemblrs63751129
gopubmedrs63751129
geneviewrs63751129
scholarrs63751129
googlers63751129
pharmgkbrs63751129
gwascentralrs63751129
openSNPrs63751129
23andMers63751129
23andMe allrs63751129
SNP Nexus

SNPshotrs63751129
SNPdbers63751129
MSV3drs63751129
GWAS Ctlgrs63751129
Max Magnitude0
ClinVar
Risk rs63751129(;)
Alt rs63751129(;)
Reference rs63751129(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702213delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076293.2,