rs587777755

Orientation

plus

Stabilized

plus

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

Make rs587777755(A;G)

Make rs587777755(G;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

32128483

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs587777755
dbSNP (classic)	rs587777755
ClinGen	rs587777755
ebi	rs587777755
HLI	rs587777755
Exac	rs587777755
Gnomad	rs587777755
Varsome	rs587777755
LitVar	rs587777755
Map	rs587777755
PheGenI	rs587777755
Biobank	rs587777755
1000 genomes	rs587777755
hgdp	rs587777755
ensembl	rs587777755
geneview	rs587777755
scholar	rs587777755
google	rs587777755
pharmgkb	rs587777755
gwascentral	rs587777755
openSNP	rs587777755
23andMe	rs587777755
SNPshot	rs587777755
SNPdbe	rs587777755
MSV3d	rs587777755
GWAS Ctlg	rs587777755

Max Magnitude

0

ClinVar
Risk	rs587777755(G;G)
Alt	rs587777755(G;G)
Reference	Rs587777755(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.32353552A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006020.2,