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rs63750741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750741(C;C)
Make rs63750741(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799329
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750741
ebirs63750741
HLIrs63750741
Exacrs63750741
Varsomers63750741
Maprs63750741
PheGenIrs63750741
hapmaprs63750741
1000 genomesrs63750741
hgdprs63750741
ensemblrs63750741
gopubmedrs63750741
geneviewrs63750741
scholarrs63750741
googlers63750741
pharmgkbrs63750741
gwascentralrs63750741
openSNPrs63750741
23andMers63750741
23andMe allrs63750741
SNP Nexus

SNPshotrs63750741
SNPdbers63750741
MSV3drs63750741
GWAS Ctlgrs63750741
Max Magnitude0
ClinVar
Risk rs63750741(C;C)
Alt rs63750741(C;C)
Reference rs63750741(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026468T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074651.2,