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rs63750996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750996(C;T)
Make rs63750996(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47798689
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750996
ebirs63750996
HLIrs63750996
Exacrs63750996
Varsomers63750996
Maprs63750996
PheGenIrs63750996
hapmaprs63750996
1000 genomesrs63750996
hgdprs63750996
ensemblrs63750996
gopubmedrs63750996
geneviewrs63750996
scholarrs63750996
googlers63750996
pharmgkbrs63750996
gwascentralrs63750996
openSNPrs63750996
23andMers63750996
23andMe allrs63750996
SNP Nexus

SNPshotrs63750996
SNPdbers63750996
MSV3drs63750996
GWAS Ctlgrs63750996
Max Magnitude0
ClinVar
Risk rs63750996(T;T)
Alt rs63750996(T;T)
Reference rs63750996(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025828C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075026.2,