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rs63750140

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750140(C;T)
Make rs63750140(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47800798
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750140
ebirs63750140
HLIrs63750140
Exacrs63750140
Varsomers63750140
Maprs63750140
PheGenIrs63750140
hapmaprs63750140
1000 genomesrs63750140
hgdprs63750140
ensemblrs63750140
gopubmedrs63750140
geneviewrs63750140
scholarrs63750140
googlers63750140
pharmgkbrs63750140
gwascentralrs63750140
openSNPrs63750140
23andMers63750140
23andMe allrs63750140
SNP Nexus

SNPshotrs63750140
SNPdbers63750140
MSV3drs63750140
GWAS Ctlgrs63750140
Max Magnitude0
ClinVar
Risk rs63750140(T;T)
Alt rs63750140(T;T)
Reference rs63750140(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027937C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074783.2,