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rs200737038

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200737038(A;A)
Make rs200737038(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position64616207
GeneCYP7B1
is asnp
is mentioned by
dbSNPrs200737038
ebirs200737038
HLIrs200737038
Exacrs200737038
Varsomers200737038
Maprs200737038
PheGenIrs200737038
hapmaprs200737038
1000 genomesrs200737038
hgdprs200737038
ensemblrs200737038
gopubmedrs200737038
geneviewrs200737038
scholarrs200737038
googlers200737038
pharmgkbrs200737038
gwascentralrs200737038
openSNPrs200737038
23andMers200737038
23andMe allrs200737038
SNP Nexus

SNPshotrs200737038
SNPdbers200737038
MSV3drs200737038
GWAS Ctlgrs200737038
Max Magnitude0
ClinVar
Risk rs200737038(A;A)
Alt rs200737038(A;A)
Reference rs200737038(G;G)
Significance Pathogenic
Disease Spastic paraplegia Inborn genetic diseases
Variation info
Gene CYP7B1
CLNDBN Spastic paraplegia Inborn genetic diseases
Reversed 0
HGVS NC_000008.10:g.65528764G>A
CLNSRC
CLNACC RCV000206556.1, RCV000210595.1,