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rs762984907

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs762984907(A;T)
Make rs762984907(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position44564583
GeneSPG11
is asnp
is mentioned by
dbSNPrs762984907
ebirs762984907
HLIrs762984907
Exacrs762984907
Varsomers762984907
Maprs762984907
PheGenIrs762984907
hapmaprs762984907
1000 genomesrs762984907
hgdprs762984907
ensemblrs762984907
gopubmedrs762984907
geneviewrs762984907
scholarrs762984907
googlers762984907
pharmgkbrs762984907
gwascentralrs762984907
openSNPrs762984907
23andMers762984907
23andMe allrs762984907
SNP Nexus

SNPshotrs762984907
SNPdbers762984907
MSV3drs762984907
GWAS Ctlgrs762984907
Max Magnitude0
ClinVar
Risk rs762984907(T;T)
Alt rs762984907(T;T)
Reference rs762984907(A;A)
Significance Probable-Pathogenic
Disease Spastic paraplegia 11
Variation info
Gene SPG11
CLNDBN Spastic paraplegia 11, autosomal recessive
Reversed 0
HGVS NC_000015.9:g.44856781A>T
CLNSRC
CLNACC RCV000196229.1,