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rs267606758

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606758(A;A)
Make rs267606758(A;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position64596755
GeneCYP7B1
is asnp
is mentioned by
dbSNPrs267606758
ebirs267606758
HLIrs267606758
Exacrs267606758
Varsomers267606758
Maprs267606758
PheGenIrs267606758
hapmaprs267606758
1000 genomesrs267606758
hgdprs267606758
ensemblrs267606758
gopubmedrs267606758
geneviewrs267606758
scholarrs267606758
googlers267606758
pharmgkbrs267606758
gwascentralrs267606758
openSNPrs267606758
23andMers267606758
23andMe allrs267606758
SNP Nexus

SNPshotrs267606758
SNPdbers267606758
MSV3drs267606758
GWAS Ctlgrs267606758
Max Magnitude0
ClinVar
Risk rs267606758(A;A)
Alt rs267606758(A;A)
Reference rs267606758(T;T)
Significance Pathogenic
Disease Spastic paraplegia 5A
Variation info
Gene CYP7B1
CLNDBN Spastic paraplegia 5A
Reversed 1
HGVS NC_000008.10:g.65509312A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006480.2,