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rs1064796765

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome14
Position102002950
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs1064796765
dbSNP (old)rs1064796765
ClinGenrs1064796765
ebirs1064796765
HLIrs1064796765
Exacrs1064796765
Gnomadrs1064796765
Varsomers1064796765
Maprs1064796765
PheGenIrs1064796765
Biobankrs1064796765
1000 genomesrs1064796765
hgdprs1064796765
ensemblrs1064796765
gopubmedrs1064796765
geneviewrs1064796765
scholarrs1064796765
googlers1064796765
pharmgkbrs1064796765
gwascentralrs1064796765
openSNPrs1064796765
23andMers1064796765
23andMe allrs1064796765
SNPshotrs1064796765
SNPdbers1064796765
MSV3drs1064796765
GWAS Ctlgrs1064796765
Max Magnitude0
ClinVar
Risk rs1064796765(A;A)
Alt rs1064796765(A;A)
Reference Rs1064796765(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102469287G>A
CLNSRC
CLNACC RCV000481138.1,