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

rs63750986

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750986(-;-)
Make rs63750986(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463101
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750986
ebirs63750986
HLIrs63750986
Exacrs63750986
Varsomers63750986
Maprs63750986
PheGenIrs63750986
hapmaprs63750986
1000 genomesrs63750986
hgdprs63750986
ensemblrs63750986
gopubmedrs63750986
geneviewrs63750986
scholarrs63750986
googlers63750986
pharmgkbrs63750986
gwascentralrs63750986
openSNPrs63750986
23andMers63750986
23andMe allrs63750986
SNP Nexus

SNPshotrs63750986
SNPdbers63750986
MSV3drs63750986
GWAS Ctlgrs63750986
Max Magnitude0
ClinVar
Risk rs63750986(;)
Alt rs63750986(;)
Reference rs63750986(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690240delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076167.2,