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rs797044918

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs797044918(-;-)
Make rs797044918(-;AAG)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position102029930
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs797044918
ClinGenrs797044918
ebirs797044918
HLIrs797044918
Exacrs797044918
Varsomers797044918
Maprs797044918
PheGenIrs797044918
hapmaprs797044918
1000 genomesrs797044918
hgdprs797044918
ensemblrs797044918
gopubmedrs797044918
geneviewrs797044918
scholarrs797044918
googlers797044918
pharmgkbrs797044918
gwascentralrs797044918
openSNPrs797044918
23andMers797044918
23andMe allrs797044918
SNP Nexus

SNPshotrs797044918
SNPdbers797044918
MSV3drs797044918
GWAS Ctlgrs797044918
Max Magnitude0
ClinVar
Risk rs797044918(-;-)
Alt rs797044918(-;-)
Reference Rs797044918(AAG;AAG)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DYNC1H1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000014.8:g.102496267_102496269delAAG
CLNSRC
CLNACC RCV000190753.1,