rs863224515

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs863224515(-;-)

Make rs863224515(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

32115756

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs863224515
dbSNP (classic)	rs863224515
ClinGen	rs863224515
ebi	rs863224515
HLI	rs863224515
Exac	rs863224515
Gnomad	rs863224515
Varsome	rs863224515
LitVar	rs863224515
Map	rs863224515
PheGenI	rs863224515
Biobank	rs863224515
1000 genomes	rs863224515
hgdp	rs863224515
ensembl	rs863224515
geneview	rs863224515
scholar	rs863224515
google	rs863224515
pharmgkb	rs863224515
gwascentral	rs863224515
openSNP	rs863224515
23andMe	rs863224515
SNPshot	rs863224515
SNPdbe	rs863224515
MSV3d	rs863224515
GWAS Ctlg	rs863224515

Max Magnitude

0

ClinVar
Risk	rs863224515(-;-)
Alt	rs863224515(-;-)
Reference	Rs863224515(C;C)
Significance	Pathogenic
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.32340825delC
CLNSRC
CLNACC	RCV000195823.1,