Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509411

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509411(A;A)
Make rs397509411(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position102033136
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs397509411
ebirs397509411
HLIrs397509411
Exacrs397509411
Varsomers397509411
Maprs397509411
PheGenIrs397509411
hapmaprs397509411
1000 genomesrs397509411
hgdprs397509411
ensemblrs397509411
gopubmedrs397509411
geneviewrs397509411
scholarrs397509411
googlers397509411
pharmgkbrs397509411
gwascentralrs397509411
openSNPrs397509411
23andMers397509411
23andMe allrs397509411
SNP Nexus

SNPshotrs397509411
SNPdbers397509411
MSV3drs397509411
GWAS Ctlgrs397509411
Max Magnitude0
ClinVar
Risk rs397509411(A;A)
Alt rs397509411(A;A)
Reference rs397509411(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DYNC1H1
CLNDBN Mental retardation, autosomal dominant 13
Reversed 0
HGVS NC_000014.8:g.102499473G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000049271.2,