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

rs587777222

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777222(C;C)
Make rs587777222(C;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position64615194
GeneCYP7B1
is asnp
is mentioned by
dbSNPrs587777222
ebirs587777222
HLIrs587777222
Exacrs587777222
Varsomers587777222
Maprs587777222
PheGenIrs587777222
hapmaprs587777222
1000 genomesrs587777222
hgdprs587777222
ensemblrs587777222
gopubmedrs587777222
geneviewrs587777222
scholarrs587777222
googlers587777222
pharmgkbrs587777222
gwascentralrs587777222
openSNPrs587777222
23andMers587777222
23andMe allrs587777222
SNP Nexus

SNPshotrs587777222
SNPdbers587777222
MSV3drs587777222
GWAS Ctlgrs587777222
Max Magnitude0
ClinVar
Risk rs587777222(C;C)
Alt rs587777222(C;C)
Reference rs587777222(T;T)
Significance Pathogenic
Disease Spastic paraplegia 5A Spastic paraplegia
Variation info
Gene CYP7B1
CLNDBN Spastic paraplegia 5A Spastic paraplegia
Reversed 0
HGVS NC_000008.10:g.65527751T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000106302.3, RCV000200232.2,