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rs797044928

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044928(A;A)
Make rs797044928(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position102032421
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs797044928
ebirs797044928
HLIrs797044928
Exacrs797044928
Varsomers797044928
Maprs797044928
PheGenIrs797044928
hapmaprs797044928
1000 genomesrs797044928
hgdprs797044928
ensemblrs797044928
gopubmedrs797044928
geneviewrs797044928
scholarrs797044928
googlers797044928
pharmgkbrs797044928
gwascentralrs797044928
openSNPrs797044928
23andMers797044928
23andMe allrs797044928
SNP Nexus

SNPshotrs797044928
SNPdbers797044928
MSV3drs797044928
GWAS Ctlgrs797044928
Max Magnitude0
ClinVar
Risk rs797044928(A;A)
Alt rs797044928(A;A)
Reference rs797044928(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DYNC1H1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000014.8:g.102498758G>A
CLNSRC
CLNACC RCV000190767.1,