Have questions? Visit https://www.reddit.com/r/SNPedia

rs752623413

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs752623413(C;C)
Make rs752623413(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89556933
GeneSPG7
is asnp
is mentioned by
dbSNPrs752623413
ebirs752623413
HLIrs752623413
Exacrs752623413
Varsomers752623413
Maprs752623413
PheGenIrs752623413
hapmaprs752623413
1000 genomesrs752623413
hgdprs752623413
ensemblrs752623413
gopubmedrs752623413
geneviewrs752623413
scholarrs752623413
googlers752623413
pharmgkbrs752623413
gwascentralrs752623413
openSNPrs752623413
23andMers752623413
23andMe allrs752623413
SNP Nexus

SNPshotrs752623413
SNPdbers752623413
MSV3drs752623413
GWAS Ctlgrs752623413
Max Magnitude0
ClinVar
Risk rs752623413(C;C)
Alt rs752623413(C;C)
Reference rs752623413(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL13 SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89623341T>C
CLNSRC
CLNACC RCV000198819.1,