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rs559906913

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs559906913(G;T)
Make rs559906913(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89532617
GeneSPG7
is asnp
is mentioned by
dbSNPrs559906913
ebirs559906913
HLIrs559906913
Exacrs559906913
Varsomers559906913
Maprs559906913
PheGenIrs559906913
hapmaprs559906913
1000 genomesrs559906913
hgdprs559906913
ensemblrs559906913
gopubmedrs559906913
geneviewrs559906913
scholarrs559906913
googlers559906913
pharmgkbrs559906913
gwascentralrs559906913
openSNPrs559906913
23andMers559906913
23andMe allrs559906913
SNP Nexus

SNPshotrs559906913
SNPdbers559906913
MSV3drs559906913
GWAS Ctlgrs559906913
Max Magnitude0
ClinVar
Risk rs559906913(A,T;A,T)
Alt rs559906913(A,T;A,T)
Reference rs559906913(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89599025G>T
CLNSRC
CLNACC RCV000196196.2,