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rs372981030

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs372981030(A;T)
Make rs372981030(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89550505
GeneSPG7
is asnp
is mentioned by
dbSNPrs372981030
ebirs372981030
HLIrs372981030
Exacrs372981030
Varsomers372981030
Maprs372981030
PheGenIrs372981030
hapmaprs372981030
1000 genomesrs372981030
hgdprs372981030
ensemblrs372981030
gopubmedrs372981030
geneviewrs372981030
scholarrs372981030
googlers372981030
pharmgkbrs372981030
gwascentralrs372981030
openSNPrs372981030
23andMers372981030
23andMe allrs372981030
SNP Nexus

SNPshotrs372981030
SNPdbers372981030
MSV3drs372981030
GWAS Ctlgrs372981030
Max Magnitude0
ClinVar
Risk rs372981030(T;T)
Alt rs372981030(T;T)
Reference rs372981030(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL13 SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89616913A>T
CLNSRC
CLNACC RCV000198266.2,