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rs748309520

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs748309520(A;A)
Make rs748309520(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89531903
GeneSPG7
is asnp
is mentioned by
dbSNPrs748309520
ebirs748309520
HLIrs748309520
Exacrs748309520
Varsomers748309520
Maprs748309520
PheGenIrs748309520
hapmaprs748309520
1000 genomesrs748309520
hgdprs748309520
ensemblrs748309520
gopubmedrs748309520
geneviewrs748309520
scholarrs748309520
googlers748309520
pharmgkbrs748309520
gwascentralrs748309520
openSNPrs748309520
23andMers748309520
23andMe allrs748309520
SNP Nexus

SNPshotrs748309520
SNPdbers748309520
MSV3drs748309520
GWAS Ctlgrs748309520
Max Magnitude0
ClinVar
Risk rs748309520(A;A)
Alt rs748309520(A;A)
Reference rs748309520(G;G)
Significance Other
Disease Spastic paraplegia 7
Variation info
Gene SPG7
CLNDBN Spastic paraplegia 7
Reversed 0
HGVS NC_000016.9:g.89598311G>A
CLNSRC
CLNACC RCV000206709.2,