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rs63750200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750200(C;T)
Make rs63750200(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475042
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750200
ebirs63750200
HLIrs63750200
Exacrs63750200
Varsomers63750200
Maprs63750200
PheGenIrs63750200
hapmaprs63750200
1000 genomesrs63750200
hgdprs63750200
ensemblrs63750200
gopubmedrs63750200
geneviewrs63750200
scholarrs63750200
googlers63750200
pharmgkbrs63750200
gwascentralrs63750200
openSNPrs63750200
23andMers63750200
23andMe allrs63750200
SNP Nexus

SNPshotrs63750200
SNPdbers63750200
MSV3drs63750200
GWAS Ctlgrs63750200
Max Magnitude0
ClinVar
Risk rs63750200(T;T)
Alt rs63750200(T;T)
Reference rs63750200(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702181C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076282.2,