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rs72547552

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72547552(A;A)
Make rs72547552(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89550559
GeneSPG7
is asnp
is mentioned by
dbSNPrs72547552
ebirs72547552
HLIrs72547552
Exacrs72547552
Varsomers72547552
Maprs72547552
PheGenIrs72547552
hapmaprs72547552
1000 genomesrs72547552
hgdprs72547552
ensemblrs72547552
gopubmedrs72547552
geneviewrs72547552
scholarrs72547552
googlers72547552
pharmgkbrs72547552
gwascentralrs72547552
openSNPrs72547552
23andMers72547552
23andMe allrs72547552
SNP Nexus

SNPshotrs72547552
SNPdbers72547552
MSV3drs72547552
GWAS Ctlgrs72547552
Max Magnitude0
ClinVar
Risk rs72547552(A;A)
Alt rs72547552(A;A)
Reference rs72547552(G;G)
Significance Probable-Pathogenic
Disease Spastic paraplegia 7
Variation info
Gene RPL13 SPG7
CLNDBN Spastic paraplegia 7
Reversed 0
HGVS NC_000016.9:g.89616967G>A
CLNSRC
CLNACC RCV000198892.1,