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rs149797758

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs149797758(C;C)
Make rs149797758(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89524153
GeneSPG7
is asnp
is mentioned by
dbSNPrs149797758
ebirs149797758
HLIrs149797758
Exacrs149797758
Varsomers149797758
Maprs149797758
PheGenIrs149797758
hapmaprs149797758
1000 genomesrs149797758
hgdprs149797758
ensemblrs149797758
gopubmedrs149797758
geneviewrs149797758
scholarrs149797758
googlers149797758
pharmgkbrs149797758
gwascentralrs149797758
openSNPrs149797758
23andMers149797758
23andMe allrs149797758
SNP Nexus

SNPshotrs149797758
SNPdbers149797758
MSV3drs149797758
GWAS Ctlgrs149797758
Max Magnitude0
ClinVar
Risk rs149797758(C;C)
Alt rs149797758(C;C)
Reference rs149797758(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89590561T>C
CLNSRC
CLNACC RCV000197458.1,