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rs201689565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201689565(A;G)
Make rs201689565(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position44584299
GeneSPG11
is asnp
is mentioned by
dbSNPrs201689565
dbSNP (old)rs201689565
ClinGenrs201689565
ebirs201689565
HLIrs201689565
Exacrs201689565
Gnomadrs201689565
Varsomers201689565
LitVarrs201689565
Maprs201689565
PheGenIrs201689565
Biobankrs201689565
1000 genomesrs201689565
hgdprs201689565
ensemblrs201689565
gopubmedrs201689565
geneviewrs201689565
scholarrs201689565
googlers201689565
pharmgkbrs201689565
gwascentralrs201689565
openSNPrs201689565
23andMers201689565
23andMe allrs201689565
SNPshotrs201689565
SNPdbers201689565
MSV3drs201689565
GWAS Ctlgrs201689565
Max Magnitude0
ClinVar
Risk rs201689565(G;G)
Alt rs201689565(G;G)
Reference Rs201689565(A;A)
Significance Probable-Pathogenic
Disease Difficulty walking Gait disturbance Generalized hyperreflexia Spastic paraparesis
Variation info
Gene SPG11
CLNDBN Difficulty walking Gait disturbance Generalized hyperreflexia Spastic paraparesis
Reversed 0
HGVS NC_000015.9:g.44876497A>G
CLNSRC
CLNACC RCV000414944.1,