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rs879254021

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879254021(C;G)
Make rs879254021(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position102040629
GeneDYNC1H1, LOC107984661
is asnp
is mentioned by
dbSNPrs879254021
dbSNP (classic)rs879254021
ClinGenrs879254021
ebirs879254021
HLIrs879254021
Exacrs879254021
Gnomadrs879254021
Varsomers879254021
LitVarrs879254021
Maprs879254021
PheGenIrs879254021
Biobankrs879254021
1000 genomesrs879254021
hgdprs879254021
ensemblrs879254021
geneviewrs879254021
scholarrs879254021
googlers879254021
pharmgkbrs879254021
gwascentralrs879254021
openSNPrs879254021
23andMers879254021
SNPshotrs879254021
SNPdbers879254021
MSV3drs879254021
GWAS Ctlgrs879254021
Max Magnitude0
ClinVar
Risk rs879254021(G;G)
Alt rs879254021(G;G)
Reference Rs879254021(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102506966C>G
CLNSRC
CLNACC RCV000235365.1,