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rs587777425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777425(A;A)
Make rs587777425(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position160237145
GeneDCAF8
is asnp
is mentioned by
dbSNPrs587777425
ebirs587777425
HLIrs587777425
Exacrs587777425
Varsomers587777425
Maprs587777425
PheGenIrs587777425
hapmaprs587777425
1000 genomesrs587777425
hgdprs587777425
ensemblrs587777425
gopubmedrs587777425
geneviewrs587777425
scholarrs587777425
googlers587777425
pharmgkbrs587777425
gwascentralrs587777425
openSNPrs587777425
23andMers587777425
23andMe allrs587777425
SNP Nexus

SNPshotrs587777425
SNPdbers587777425
MSV3drs587777425
GWAS Ctlgrs587777425
Max Magnitude0
ClinVar
Risk rs587777425(A;A)
Alt rs587777425(A;A)
Reference rs587777425(G;G)
Significance Pathogenic
Disease Giant axonal neuropathy 2
Variation info
Gene DCAF8
CLNDBN Giant axonal neuropathy 2, autosomal dominant
Reversed 0
HGVS NC_000001.10:g.160206935G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000119848.2,