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

rs63750362

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750362(-;-)
Make rs63750362(-;T)
Make rs63750362(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463138
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750362
ebirs63750362
HLIrs63750362
Exacrs63750362
Varsomers63750362
Maprs63750362
PheGenIrs63750362
hapmaprs63750362
1000 genomesrs63750362
hgdprs63750362
ensemblrs63750362
gopubmedrs63750362
geneviewrs63750362
scholarrs63750362
googlers63750362
pharmgkbrs63750362
gwascentralrs63750362
openSNPrs63750362
23andMers63750362
23andMe allrs63750362
SNP Nexus

SNPshotrs63750362
SNPdbers63750362
MSV3drs63750362
GWAS Ctlgrs63750362
Max Magnitude0
ClinVar
Risk rs63750362(T;T)
Alt rs63750362(T;T)
Reference rs63750362(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690277dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076176.2,