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rs587777200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777200(G;T)
Make rs587777200(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position95844582
GeneENTPD1, ENTPD1-AS1
is asnp
is mentioned by
dbSNPrs587777200
ebirs587777200
HLIrs587777200
Exacrs587777200
Varsomers587777200
Maprs587777200
PheGenIrs587777200
hapmaprs587777200
1000 genomesrs587777200
hgdprs587777200
ensemblrs587777200
gopubmedrs587777200
geneviewrs587777200
scholarrs587777200
googlers587777200
pharmgkbrs587777200
gwascentralrs587777200
openSNPrs587777200
23andMers587777200
23andMe allrs587777200
SNP Nexus

SNPshotrs587777200
SNPdbers587777200
MSV3drs587777200
GWAS Ctlgrs587777200
Max Magnitude0
ClinVar
Risk rs587777200(A,T;A,T)
Alt rs587777200(A,T;A,T)
Reference rs587777200(G;G)
Significance Pathogenic
Disease Spastic paraplegia 64
Variation info
Gene ENTPD1-AS1 ENTPD1
CLNDBN Spastic paraplegia 64, autosomal recessive
Reversed 0
HGVS NC_000010.10:g.97604339G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087330.3,