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rs67586389

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs67586389(A;A)
Make rs67586389(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position74378067
GeneDCTN1
is asnp
is mentioned by
dbSNPrs67586389
ebirs67586389
HLIrs67586389
Exacrs67586389
Varsomers67586389
Maprs67586389
PheGenIrs67586389
hapmaprs67586389
1000 genomesrs67586389
hgdprs67586389
ensemblrs67586389
gopubmedrs67586389
geneviewrs67586389
scholarrs67586389
googlers67586389
pharmgkbrs67586389
gwascentralrs67586389
openSNPrs67586389
23andMers67586389
23andMe allrs67586389
SNP Nexus

SNPshotrs67586389
SNPdbers67586389
MSV3drs67586389
GWAS Ctlgrs67586389
Max Magnitude0
ClinVar
Risk rs67586389(A,C;A,C)
Alt rs67586389(A,C;A,C)
Reference rs67586389(G;G)
Significance Pathogenic
Disease Perry syndrome
Variation info
Gene DCTN1
CLNDBN Perry syndrome
Reversed 1
HGVS NC_000002.11:g.74605194C>G; NC_000002.11:g.74605194C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000020577.1, RCV000020576.3,