rs587777753

Orientation

plus

Stabilized

plus

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

Make rs587777753(-;A)

Make rs587777753(A;A)

Reference

GRCh38 38.1/142

Chromosome

2

Position

32087529

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs587777753
dbSNP (classic)	rs587777753
ClinGen	rs587777753
ebi	rs587777753
HLI	rs587777753
Exac	rs587777753
Gnomad	rs587777753
Varsome	rs587777753
LitVar	rs587777753
Map	rs587777753
PheGenI	rs587777753
Biobank	rs587777753
1000 genomes	rs587777753
hgdp	rs587777753
ensembl	rs587777753
geneview	rs587777753
scholar	rs587777753
google	rs587777753
pharmgkb	rs587777753
gwascentral	rs587777753
openSNP	rs587777753
23andMe	rs587777753
SNPshot	rs587777753
SNPdbe	rs587777753
MSV3d	rs587777753
GWAS Ctlg	rs587777753

Max Magnitude

0

ClinVar
Risk	rs587777753(A;A)
Alt	rs587777753(A;A)
Reference	Rs587777753(-;-)
Significance	Pathogenic
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.32312598dupA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006017.2,