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rs869312924

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312924(A;A)
Make rs869312924(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position103154606
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs869312924
ebirs869312924
HLIrs869312924
Exacrs869312924
Varsomers869312924
Maprs869312924
PheGenIrs869312924
hapmaprs869312924
1000 genomesrs869312924
hgdprs869312924
ensemblrs869312924
gopubmedrs869312924
geneviewrs869312924
scholarrs869312924
googlers869312924
pharmgkbrs869312924
gwascentralrs869312924
openSNPrs869312924
23andMers869312924
23andMe allrs869312924
SNP Nexus

SNPshotrs869312924
SNPdbers869312924
MSV3drs869312924
GWAS Ctlgrs869312924
Max Magnitude0
ClinVar
Risk rs869312924(A;A)
Alt rs869312924(A;A)
Reference rs869312924(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DYNC2H1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.103025335G>A
CLNSRC
CLNACC RCV000210659.1,