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rs864622111

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864622111(A;G)
Make rs864622111(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position103243691
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs864622111
ebirs864622111
HLIrs864622111
Exacrs864622111
Varsomers864622111
Maprs864622111
PheGenIrs864622111
hapmaprs864622111
1000 genomesrs864622111
hgdprs864622111
ensemblrs864622111
gopubmedrs864622111
geneviewrs864622111
scholarrs864622111
googlers864622111
pharmgkbrs864622111
gwascentralrs864622111
openSNPrs864622111
23andMers864622111
23andMe allrs864622111
SNP Nexus

SNPshotrs864622111
SNPdbers864622111
MSV3drs864622111
GWAS Ctlgrs864622111
Max Magnitude0
ClinVar
Risk rs864622111(G;G)
Alt rs864622111(G;G)
Reference rs864622111(A;A)
Significance Probable-Pathogenic
Disease Jeune thoracic dystrophy
Variation info
Gene DYNC2H1
CLNDBN Jeune thoracic dystrophy
Reversed 0
HGVS NC_000011.9:g.103114420A>G
CLNSRC
CLNACC RCV000206518.1,