rs587777752

Orientation

plus

Stabilized

plus

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

Make rs587777752(A;G)

Make rs587777752(G;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

32147216

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs587777752
dbSNP (classic)	rs587777752
ClinGen	rs587777752
ebi	rs587777752
HLI	rs587777752
Exac	rs587777752
Gnomad	rs587777752
Varsome	rs587777752
LitVar	rs587777752
Map	rs587777752
PheGenI	rs587777752
Biobank	rs587777752
1000 genomes	rs587777752
hgdp	rs587777752
ensembl	rs587777752
geneview	rs587777752
scholar	rs587777752
google	rs587777752
pharmgkb	rs587777752
gwascentral	rs587777752
openSNP	rs587777752
23andMe	rs587777752
SNPshot	rs587777752
SNPdbe	rs587777752
MSV3d	rs587777752
GWAS Ctlg	rs587777752

Max Magnitude

0

ClinVar
Risk	rs587777752(G;G)
Alt	rs587777752(G;G)
Reference	Rs587777752(A;A)
Significance	Pathogenic
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.32372285A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006015.2,