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rs879254019

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879254019(C;T)
Make rs879254019(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position102015162
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs879254019
dbSNP (classic)rs879254019
ClinGenrs879254019
ebirs879254019
HLIrs879254019
Exacrs879254019
Gnomadrs879254019
Varsomers879254019
LitVarrs879254019
Maprs879254019
PheGenIrs879254019
Biobankrs879254019
1000 genomesrs879254019
hgdprs879254019
ensemblrs879254019
geneviewrs879254019
scholarrs879254019
googlers879254019
pharmgkbrs879254019
gwascentralrs879254019
openSNPrs879254019
23andMers879254019
SNPshotrs879254019
SNPdbers879254019
MSV3drs879254019
GWAS Ctlgrs879254019
Max Magnitude0
ClinVar
Risk rs879254019(T;T)
Alt rs879254019(T;T)
Reference Rs879254019(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102481499C>T
CLNSRC
CLNACC RCV000236944.1,