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rs121908612

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908612(C;C)
Make rs121908612(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position64615894
GeneCYP7B1
is asnp
is mentioned by
dbSNPrs121908612
ebirs121908612
HLIrs121908612
Exacrs121908612
Varsomers121908612
Maprs121908612
PheGenIrs121908612
hapmaprs121908612
1000 genomesrs121908612
hgdprs121908612
ensemblrs121908612
gopubmedrs121908612
geneviewrs121908612
scholarrs121908612
googlers121908612
pharmgkbrs121908612
gwascentralrs121908612
openSNPrs121908612
23andMers121908612
23andMe allrs121908612
SNP Nexus

SNPshotrs121908612
SNPdbers121908612
MSV3drs121908612
GWAS Ctlgrs121908612
Max Magnitude0
OMIM603711
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908612(C;C)
Alt rs121908612(C;C)
Reference rs121908612(T;T)
Significance Pathogenic
Disease Spastic paraplegia 5A
Variation info
Gene CYP7B1
CLNDBN Spastic paraplegia 5A
Reversed 1
HGVS NC_000008.10:g.65528451A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006478.2,