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rs63750312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750312(G;G)
Make rs63750312(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475122
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750312
ClinGenrs63750312
ebirs63750312
HLIrs63750312
Exacrs63750312
Varsomers63750312
Maprs63750312
PheGenIrs63750312
hapmaprs63750312
1000 genomesrs63750312
hgdprs63750312
ensemblrs63750312
gopubmedrs63750312
geneviewrs63750312
scholarrs63750312
googlers63750312
pharmgkbrs63750312
gwascentralrs63750312
openSNPrs63750312
23andMers63750312
23andMe allrs63750312
SNP Nexus

SNPshotrs63750312
SNPdbers63750312
MSV3drs63750312
GWAS Ctlgrs63750312
Max Magnitude0
ClinVar
Risk rs63750312(G;G)
Alt rs63750312(G;G)
Reference Rs63750312(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702261T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076303.2,