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

rs748555510

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748555510(C;T)
Make rs748555510(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89544731
GeneSPG7
is asnp
is mentioned by
dbSNPrs748555510
ebirs748555510
HLIrs748555510
Exacrs748555510
Varsomers748555510
Maprs748555510
PheGenIrs748555510
hapmaprs748555510
1000 genomesrs748555510
hgdprs748555510
ensemblrs748555510
gopubmedrs748555510
geneviewrs748555510
scholarrs748555510
googlers748555510
pharmgkbrs748555510
gwascentralrs748555510
openSNPrs748555510
23andMers748555510
23andMe allrs748555510
SNP Nexus

SNPshotrs748555510
SNPdbers748555510
MSV3drs748555510
GWAS Ctlgrs748555510
Max Magnitude0
ClinVar
Risk rs748555510(T;T)
Alt rs748555510(T;T)
Reference rs748555510(C;C)
Significance Pathogenic
Disease Spastic paraplegia 7
Variation info
Gene SPG7
CLNDBN Spastic paraplegia 7
Reversed 0
HGVS NC_000016.9:g.89611139C>T
CLNSRC
CLNACC RCV000196592.1,