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rs141431913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141431913(C;T)
Make rs141431913(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position107950250
GeneCYP2U1
is asnp
is mentioned by
dbSNPrs141431913
ebirs141431913
HLIrs141431913
Exacrs141431913
Varsomers141431913
Maprs141431913
PheGenIrs141431913
hapmaprs141431913
1000 genomesrs141431913
hgdprs141431913
ensemblrs141431913
gopubmedrs141431913
geneviewrs141431913
scholarrs141431913
googlers141431913
pharmgkbrs141431913
gwascentralrs141431913
openSNPrs141431913
23andMers141431913
23andMe allrs141431913
SNP Nexus

SNPshotrs141431913
SNPdbers141431913
MSV3drs141431913
GWAS Ctlgrs141431913
Max Magnitude0
ClinVar
Risk rs141431913(T;T)
Alt rs141431913(T;T)
Reference rs141431913(C;C)
Significance Pathogenic
Disease Spastic paraplegia 56
Variation info
Gene CYP2U1
CLNDBN Spastic paraplegia 56, autosomal recessive
Reversed 0
HGVS NC_000004.11:g.108871406C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032700.3,