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rs879254267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879254267(A;T)
Make rs879254267(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position101983070
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs879254267
dbSNP (classic)rs879254267
ClinGenrs879254267
ebirs879254267
HLIrs879254267
Exacrs879254267
Gnomadrs879254267
Varsomers879254267
LitVarrs879254267
Maprs879254267
PheGenIrs879254267
Biobankrs879254267
1000 genomesrs879254267
hgdprs879254267
ensemblrs879254267
geneviewrs879254267
scholarrs879254267
googlers879254267
pharmgkbrs879254267
gwascentralrs879254267
openSNPrs879254267
23andMers879254267
SNPshotrs879254267
SNPdbers879254267
MSV3drs879254267
GWAS Ctlgrs879254267
Max Magnitude0
ClinVar
Risk rs879254267(T;T)
Alt rs879254267(T;T)
Reference Rs879254267(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102449407A>T
CLNSRC
CLNACC RCV000236737.1,