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rs267607085

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607085(C;C)
Make rs267607085(C;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position89550579
GeneSPG7
is asnp
is mentioned by
dbSNPrs267607085
ebirs267607085
HLIrs267607085
Exacrs267607085
Varsomers267607085
Maprs267607085
PheGenIrs267607085
hapmaprs267607085
1000 genomesrs267607085
hgdprs267607085
ensemblrs267607085
gopubmedrs267607085
geneviewrs267607085
scholarrs267607085
googlers267607085
pharmgkbrs267607085
gwascentralrs267607085
openSNPrs267607085
23andMers267607085
23andMe allrs267607085
SNP Nexus

SNPshotrs267607085
SNPdbers267607085
MSV3drs267607085
GWAS Ctlgrs267607085
Max Magnitude0
ClinVar
Risk rs267607085(C;C)
Alt rs267607085(C;C)
Reference rs267607085(G;G)
Significance Pathogenic
Disease Spastic paraplegia 7
Variation info
Gene RPL13 SPG7
CLNDBN Spastic paraplegia 7
Reversed 0
HGVS NC_000016.9:g.89616987G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007222.4,