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rs794726906

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794726906(A;G)
Make rs794726906(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89508418
GeneLOC101927863, SPG7
is asnp
is mentioned by
dbSNPrs794726906
ebirs794726906
HLIrs794726906
Exacrs794726906
Varsomers794726906
Maprs794726906
PheGenIrs794726906
hapmaprs794726906
1000 genomesrs794726906
hgdprs794726906
ensemblrs794726906
gopubmedrs794726906
geneviewrs794726906
scholarrs794726906
googlers794726906
pharmgkbrs794726906
gwascentralrs794726906
openSNPrs794726906
23andMers794726906
23andMe allrs794726906
SNP Nexus

SNPshotrs794726906
SNPdbers794726906
MSV3drs794726906
GWAS Ctlgrs794726906
Max Magnitude0
ClinVar
Risk rs794726906(G;G)
Alt rs794726906(G;G)
Reference rs794726906(A;A)
Significance Probable-Pathogenic
Disease Spastic paraplegia 7
Variation info
Gene SPG7
CLNDBN Spastic paraplegia 7
Reversed 0
HGVS NC_000016.9:g.89574826A>G
CLNSRC
CLNACC RCV000173302.1,