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rs63750234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750234(A;A)
Make rs63750234(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476381
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750234
ebirs63750234
HLIrs63750234
Exacrs63750234
Varsomers63750234
Maprs63750234
PheGenIrs63750234
hapmaprs63750234
1000 genomesrs63750234
hgdprs63750234
ensemblrs63750234
gopubmedrs63750234
geneviewrs63750234
scholarrs63750234
googlers63750234
pharmgkbrs63750234
gwascentralrs63750234
openSNPrs63750234
23andMers63750234
23andMe allrs63750234
SNP Nexus

SNPshotrs63750234
SNPdbers63750234
MSV3drs63750234
GWAS Ctlgrs63750234
Max Magnitude0
ClinVar
Risk rs63750234(A,C;A,C)
Alt rs63750234(A,C;A,C)
Reference rs63750234(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703520G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076362.2,