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rs121908614

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908614(A;A)
Make rs121908614(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position64624493
GeneCYP7B1
is asnp
is mentioned by
dbSNPrs121908614
ebirs121908614
HLIrs121908614
Exacrs121908614
Varsomers121908614
Maprs121908614
PheGenIrs121908614
hapmaprs121908614
1000 genomesrs121908614
hgdprs121908614
ensemblrs121908614
gopubmedrs121908614
geneviewrs121908614
scholarrs121908614
googlers121908614
pharmgkbrs121908614
gwascentralrs121908614
openSNPrs121908614
23andMers121908614
23andMe allrs121908614
SNP Nexus

SNPshotrs121908614
SNPdbers121908614
MSV3drs121908614
GWAS Ctlgrs121908614
Max Magnitude0
OMIM603711
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908614(A;A)
Alt rs121908614(A;A)
Reference rs121908614(G;G)
Significance Pathogenic
Disease Spastic paraplegia 5A
Variation info
Gene CYP7B1
CLNDBN Spastic paraplegia 5A
Reversed 1
HGVS NC_000008.10:g.65537050C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006476.2,