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

rs63749975

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
(I;I) 0
(TG;TG) 0 common in clinvar
Make rs63749975(-;-)
Make rs63749975(-;TG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47480766
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749975
ebirs63749975
HLIrs63749975
Exacrs63749975
Varsomers63749975
Maprs63749975
PheGenIrs63749975
hapmaprs63749975
1000 genomesrs63749975
hgdprs63749975
ensemblrs63749975
gopubmedrs63749975
geneviewrs63749975
scholarrs63749975
googlers63749975
pharmgkbrs63749975
gwascentralrs63749975
openSNPrs63749975
23andMers63749975
23andMe allrs63749975
SNP Nexus

SNPshotrs63749975
SNPdbers63749975
MSV3drs63749975
GWAS Ctlgrs63749975
Max Magnitude0
ClinVar
Risk rs63749975(;)
Alt rs63749975(;)
Reference rs63749975(GT;GT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707905_47707906delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076496.2,