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rs63750436

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750436(-;-)
Make rs63750436(-;A)
Make rs63750436(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463088
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750436
ebirs63750436
HLIrs63750436
Exacrs63750436
Varsomers63750436
Maprs63750436
PheGenIrs63750436
hapmaprs63750436
1000 genomesrs63750436
hgdprs63750436
ensemblrs63750436
gopubmedrs63750436
geneviewrs63750436
scholarrs63750436
googlers63750436
pharmgkbrs63750436
gwascentralrs63750436
openSNPrs63750436
23andMers63750436
23andMe allrs63750436
SNP Nexus

SNPshotrs63750436
SNPdbers63750436
MSV3drs63750436
GWAS Ctlgrs63750436
Max Magnitude0
ClinVar
Risk rs63750436(A;A)
Alt rs63750436(A;A)
Reference rs63750436(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690227dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076162.2,