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rs63750780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750780(C;T)
Make rs63750780(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466699
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750780
ebirs63750780
HLIrs63750780
Exacrs63750780
Varsomers63750780
Maprs63750780
PheGenIrs63750780
hapmaprs63750780
1000 genomesrs63750780
hgdprs63750780
ensemblrs63750780
gopubmedrs63750780
geneviewrs63750780
scholarrs63750780
googlers63750780
pharmgkbrs63750780
gwascentralrs63750780
openSNPrs63750780
23andMers63750780
23andMe allrs63750780
SNP Nexus

SNPshotrs63750780
SNPdbers63750780
MSV3drs63750780
GWAS Ctlgrs63750780
Max Magnitude0
ClinVar
Risk rs63750780(T;T)
Alt rs63750780(T;T)
Reference rs63750780(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693838C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076192.2,