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rs764193290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs764193290(-;-)
Make rs764193290(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position237342163
GeneCOL6A3
is asnp
is mentioned by
dbSNPrs764193290
dbSNP (classic)rs764193290
ClinGenrs764193290
ebirs764193290
HLIrs764193290
Exacrs764193290
Gnomadrs764193290
Varsomers764193290
LitVarrs764193290
Maprs764193290
PheGenIrs764193290
Biobankrs764193290
1000 genomesrs764193290
hgdprs764193290
ensemblrs764193290
geneviewrs764193290
scholarrs764193290
googlers764193290
pharmgkbrs764193290
gwascentralrs764193290
openSNPrs764193290
23andMers764193290
SNPshotrs764193290
SNPdbers764193290
MSV3drs764193290
GWAS Ctlgrs764193290
Max Magnitude0
ClinVar
Risk rs764193290(-;-)
Alt rs764193290(-;-)
Reference Rs764193290(T;T)
Significance Probable-Pathogenic
Disease Bethlem myopathy 1 Dystonia 27 Ullrich congenital muscular dystrophy 1
Variation info
Gene COL6A3
CLNDBN Bethlem myopathy 1 Dystonia 27 Ullrich congenital muscular dystrophy 1
Reversed 0
HGVS NC_000002.11:g.238250806delT
CLNSRC
CLNACC RCV000477801.1,