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rs151249432

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151249432(C;T)
Make rs151249432(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89550557
GeneSPG7
is asnp
is mentioned by
dbSNPrs151249432
ebirs151249432
HLIrs151249432
Exacrs151249432
Varsomers151249432
Maprs151249432
PheGenIrs151249432
hapmaprs151249432
1000 genomesrs151249432
hgdprs151249432
ensemblrs151249432
gopubmedrs151249432
geneviewrs151249432
scholarrs151249432
googlers151249432
pharmgkbrs151249432
gwascentralrs151249432
openSNPrs151249432
23andMers151249432
23andMe allrs151249432
SNP Nexus

SNPshotrs151249432
SNPdbers151249432
MSV3drs151249432
GWAS Ctlgrs151249432
Max Magnitude0
ClinVar
Risk rs151249432(G,T;G,T)
Alt rs151249432(G,T;G,T)
Reference rs151249432(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL13 SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89616965C>G
CLNSRC
CLNACC RCV000197553.2,