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rs63750552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750552(G;T)
Make rs63750552(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47798797
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750552
ebirs63750552
HLIrs63750552
Exacrs63750552
Varsomers63750552
Maprs63750552
PheGenIrs63750552
hapmaprs63750552
1000 genomesrs63750552
hgdprs63750552
ensemblrs63750552
gopubmedrs63750552
geneviewrs63750552
scholarrs63750552
googlers63750552
pharmgkbrs63750552
gwascentralrs63750552
openSNPrs63750552
23andMers63750552
23andMe allrs63750552
SNP Nexus

SNPshotrs63750552
SNPdbers63750552
MSV3drs63750552
GWAS Ctlgrs63750552
Max Magnitude0
ClinVar
Risk rs63750552(T;T)
Alt rs63750552(T;T)
Reference rs63750552(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025936G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075038.2,