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rs879254164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879254164(C;T)
Make rs879254164(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position101995022
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs879254164
dbSNP (classic)rs879254164
ClinGenrs879254164
ebirs879254164
HLIrs879254164
Exacrs879254164
Gnomadrs879254164
Varsomers879254164
LitVarrs879254164
Maprs879254164
PheGenIrs879254164
Biobankrs879254164
1000 genomesrs879254164
hgdprs879254164
ensemblrs879254164
geneviewrs879254164
scholarrs879254164
googlers879254164
pharmgkbrs879254164
gwascentralrs879254164
openSNPrs879254164
23andMers879254164
SNPshotrs879254164
SNPdbers879254164
MSV3drs879254164
GWAS Ctlgrs879254164
Max Magnitude0
ClinVar
Risk rs879254164(T;T)
Alt rs879254164(T;T)
Reference Rs879254164(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102461359C>T
CLNSRC
CLNACC RCV000236857.1,