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rs587777668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777668(A;A)
Make rs587777668(A;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position123253958
GeneC12orf65
is asnp
is mentioned by
dbSNPrs587777668
ebirs587777668
HLIrs587777668
Exacrs587777668
Varsomers587777668
Maprs587777668
PheGenIrs587777668
hapmaprs587777668
1000 genomesrs587777668
hgdprs587777668
ensemblrs587777668
gopubmedrs587777668
geneviewrs587777668
scholarrs587777668
googlers587777668
pharmgkbrs587777668
gwascentralrs587777668
openSNPrs587777668
23andMers587777668
23andMe allrs587777668
SNP Nexus

SNPshotrs587777668
SNPdbers587777668
MSV3drs587777668
GWAS Ctlgrs587777668
Max Magnitude0
ClinVar
Risk rs587777668(A;A)
Alt rs587777668(A;A)
Reference rs587777668(T;T)
Significance Pathogenic
Disease Spastic paraplegia 55
Variation info
Gene C12orf65
CLNDBN Spastic paraplegia 55, autosomal recessive
Reversed 0
HGVS NC_000012.11:g.123738505T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000133581.2,