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rs767024102

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs767024102(-;-)
Make rs767024102(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position107947458
GeneCYP2U1
is asnp
is mentioned by
dbSNPrs767024102
ebirs767024102
HLIrs767024102
Exacrs767024102
Varsomers767024102
Maprs767024102
PheGenIrs767024102
hapmaprs767024102
1000 genomesrs767024102
hgdprs767024102
ensemblrs767024102
gopubmedrs767024102
geneviewrs767024102
scholarrs767024102
googlers767024102
pharmgkbrs767024102
gwascentralrs767024102
openSNPrs767024102
23andMers767024102
23andMe allrs767024102
SNP Nexus

SNPshotrs767024102
SNPdbers767024102
MSV3drs767024102
GWAS Ctlgrs767024102
Max Magnitude0
ClinVar
Risk rs767024102(;)
Alt rs767024102(;)
Reference rs767024102(AG;AG)
Significance Pathogenic
Disease Spastic paraplegia 56
Variation info
Gene CYP2U1
CLNDBN Spastic paraplegia 56, autosomal recessive
Reversed 0
HGVS NC_000004.11:g.108868614_108868615delAG
CLNSRC
CLNACC RCV000184032.1,