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rs587777136

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777136(C;T)
Make rs587777136(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position42562797
GeneCOASY
is asnp
is mentioned by
dbSNPrs587777136
ebirs587777136
HLIrs587777136
Exacrs587777136
Varsomers587777136
Maprs587777136
PheGenIrs587777136
hapmaprs587777136
1000 genomesrs587777136
hgdprs587777136
ensemblrs587777136
gopubmedrs587777136
geneviewrs587777136
scholarrs587777136
googlers587777136
pharmgkbrs587777136
gwascentralrs587777136
openSNPrs587777136
23andMers587777136
23andMe allrs587777136
SNP Nexus

SNPshotrs587777136
SNPdbers587777136
MSV3drs587777136
GWAS Ctlgrs587777136
Max Magnitude0
ClinVar
Risk rs587777136(T;T)
Alt rs587777136(T;T)
Reference rs587777136(C;C)
Significance Pathogenic
Disease Neurodegeneration with brain iron accumulation 6
Variation info
Gene COASY
CLNDBN Neurodegeneration with brain iron accumulation 6
Reversed 0
HGVS NC_000017.10:g.40714815C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087063.4,