Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777221

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777221(A;A)
Make rs587777221(A;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position64616281
GeneCYP7B1
is asnp
is mentioned by
dbSNPrs587777221
ebirs587777221
HLIrs587777221
Exacrs587777221
Varsomers587777221
Maprs587777221
PheGenIrs587777221
hapmaprs587777221
1000 genomesrs587777221
hgdprs587777221
ensemblrs587777221
gopubmedrs587777221
geneviewrs587777221
scholarrs587777221
googlers587777221
pharmgkbrs587777221
gwascentralrs587777221
openSNPrs587777221
23andMers587777221
23andMe allrs587777221
SNP Nexus

SNPshotrs587777221
SNPdbers587777221
MSV3drs587777221
GWAS Ctlgrs587777221
Max Magnitude0
ClinVar
Risk rs587777221(A,C;A,C)
Alt rs587777221(A,C;A,C)
Reference rs587777221(G;G)
Significance Pathogenic
Disease Spastic paraplegia 5A
Variation info
Gene CYP7B1
CLNDBN Spastic paraplegia 5A
Reversed 1
HGVS NC_000008.10:g.65528838C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000106301.2,