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

rs63750401

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750401(-;-)
Make rs63750401(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410143
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750401
ebirs63750401
HLIrs63750401
Exacrs63750401
Varsomers63750401
Maprs63750401
PheGenIrs63750401
hapmaprs63750401
1000 genomesrs63750401
hgdprs63750401
ensemblrs63750401
gopubmedrs63750401
geneviewrs63750401
scholarrs63750401
googlers63750401
pharmgkbrs63750401
gwascentralrs63750401
openSNPrs63750401
23andMers63750401
23andMe allrs63750401
SNP Nexus

SNPshotrs63750401
SNPdbers63750401
MSV3drs63750401
GWAS Ctlgrs63750401
Max Magnitude0
ClinVar
Risk rs63750401(;)
Alt rs63750401(;)
Reference rs63750401(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637282delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076597.2,