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rs752257333

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752257333(A;A)
Make rs752257333(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89554486
GeneSPG7
is asnp
is mentioned by
dbSNPrs752257333
ebirs752257333
HLIrs752257333
Exacrs752257333
Varsomers752257333
Maprs752257333
PheGenIrs752257333
hapmaprs752257333
1000 genomesrs752257333
hgdprs752257333
ensemblrs752257333
gopubmedrs752257333
geneviewrs752257333
scholarrs752257333
googlers752257333
pharmgkbrs752257333
gwascentralrs752257333
openSNPrs752257333
23andMers752257333
23andMe allrs752257333
SNP Nexus

SNPshotrs752257333
SNPdbers752257333
MSV3drs752257333
GWAS Ctlgrs752257333
Max Magnitude0
ClinVar
Risk rs752257333(A;A)
Alt rs752257333(A;A)
Reference rs752257333(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPL13 SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89620894G>A
CLNSRC
CLNACC RCV000200130.2,