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

rs63749930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs63749930(-;-)
Make rs63749930(-;CA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466699
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749930
ebirs63749930
HLIrs63749930
Exacrs63749930
Varsomers63749930
Maprs63749930
PheGenIrs63749930
hapmaprs63749930
1000 genomesrs63749930
hgdprs63749930
ensemblrs63749930
gopubmedrs63749930
geneviewrs63749930
scholarrs63749930
googlers63749930
pharmgkbrs63749930
gwascentralrs63749930
openSNPrs63749930
23andMers63749930
23andMe allrs63749930
SNP Nexus

SNPshotrs63749930
SNPdbers63749930
MSV3drs63749930
GWAS Ctlgrs63749930
Max Magnitude0
ClinVar
Risk rs63749930(;)
Alt rs63749930(;)
Reference rs63749930(CA;CA)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47693838_47693839delCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076193.2, RCV000235817.1,