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rs63750844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750844(G;G)
Make rs63750844(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475029
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750844
ebirs63750844
HLIrs63750844
Exacrs63750844
Varsomers63750844
Maprs63750844
PheGenIrs63750844
hapmaprs63750844
1000 genomesrs63750844
hgdprs63750844
ensemblrs63750844
gopubmedrs63750844
geneviewrs63750844
scholarrs63750844
googlers63750844
pharmgkbrs63750844
gwascentralrs63750844
openSNPrs63750844
23andMers63750844
23andMe allrs63750844
SNP Nexus

SNPshotrs63750844
SNPdbers63750844
MSV3drs63750844
GWAS Ctlgrs63750844
Max Magnitude0
ClinVar
Risk rs63750844(C,G;C,G)
Alt rs63750844(C,G;C,G)
Reference rs63750844(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702168T>C; NC_000002.11:g.47702168T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000167352.1, RCV000076279.2,