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rs63750302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750302(C;T)
Make rs63750302(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429848
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750302
ebirs63750302
HLIrs63750302
Exacrs63750302
Varsomers63750302
Maprs63750302
PheGenIrs63750302
hapmaprs63750302
1000 genomesrs63750302
hgdprs63750302
ensemblrs63750302
gopubmedrs63750302
geneviewrs63750302
scholarrs63750302
googlers63750302
pharmgkbrs63750302
gwascentralrs63750302
openSNPrs63750302
23andMers63750302
23andMe allrs63750302
SNP Nexus

SNPshotrs63750302
SNPdbers63750302
MSV3drs63750302
GWAS Ctlgrs63750302
Max Magnitude0
ClinVar
Risk rs63750302(T;T)
Alt rs63750302(T;T)
Reference rs63750302(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656987C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076054.2,