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rs864622358

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622358(A;A)
Make rs864622358(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position103143396
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs864622358
ebirs864622358
HLIrs864622358
Exacrs864622358
Varsomers864622358
Maprs864622358
PheGenIrs864622358
hapmaprs864622358
1000 genomesrs864622358
hgdprs864622358
ensemblrs864622358
gopubmedrs864622358
geneviewrs864622358
scholarrs864622358
googlers864622358
pharmgkbrs864622358
gwascentralrs864622358
openSNPrs864622358
23andMers864622358
23andMe allrs864622358
SNP Nexus

SNPshotrs864622358
SNPdbers864622358
MSV3drs864622358
GWAS Ctlgrs864622358
Max Magnitude0
ClinVar
Risk rs864622358(A;A)
Alt rs864622358(A;A)
Reference rs864622358(G;G)
Significance Pathogenic
Disease Jeune thoracic dystrophy
Variation info
Gene DYNC2H1
CLNDBN Jeune thoracic dystrophy
Reversed 0
HGVS NC_000011.9:g.103014125G>A
CLNSRC
CLNACC RCV000204107.1,