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rs797046003

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797046003(-;T)
Make rs797046003(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89529579
GeneSPG7
is asnp
is mentioned by
dbSNPrs797046003
dbSNP (old)rs797046003
ClinGenrs797046003
ebirs797046003
HLIrs797046003
Exacrs797046003
Gnomadrs797046003
Varsomers797046003
Maprs797046003
PheGenIrs797046003
Biobankrs797046003
1000 genomesrs797046003
hgdprs797046003
ensemblrs797046003
gopubmedrs797046003
geneviewrs797046003
scholarrs797046003
googlers797046003
pharmgkbrs797046003
gwascentralrs797046003
openSNPrs797046003
23andMers797046003
23andMe allrs797046003
SNP Nexus

SNPshotrs797046003
SNPdbers797046003
MSV3drs797046003
GWAS Ctlgrs797046003
Max Magnitude0
ClinVar
Risk rs797046003(T;T)
Alt rs797046003(T;T)
Reference Rs797046003(-;-)
Significance Pathogenic
Disease Spastic paraplegia 7 not provided
Variation info
Gene SPG7
CLNDBN Spastic paraplegia 7 not provided
Reversed 0
HGVS NC_000016.9:g.89595987dupT
CLNSRC
CLNACC RCV000194085.1, RCV000199034.1,