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rs63750731

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750731(-;-)
Make rs63750731(-;T)
Make rs63750731(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47805696
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750731
ebirs63750731
HLIrs63750731
Exacrs63750731
Varsomers63750731
Maprs63750731
PheGenIrs63750731
hapmaprs63750731
1000 genomesrs63750731
hgdprs63750731
ensemblrs63750731
gopubmedrs63750731
geneviewrs63750731
scholarrs63750731
googlers63750731
pharmgkbrs63750731
gwascentralrs63750731
openSNPrs63750731
23andMers63750731
23andMe allrs63750731
SNP Nexus

SNPshotrs63750731
SNPdbers63750731
MSV3drs63750731
GWAS Ctlgrs63750731
Max Magnitude0
ClinVar
Risk rs63750731(T;T)
Alt rs63750731(T;T)
Reference rs63750731(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48032835dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074895.2,