rs587777756

Orientation

plus

Stabilized

plus

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

Make rs587777756(-;T)

Make rs587777756(T;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

32136970

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs587777756
dbSNP (classic)	rs587777756
ClinGen	rs587777756
ebi	rs587777756
HLI	rs587777756
Exac	rs587777756
Gnomad	rs587777756
Varsome	rs587777756
LitVar	rs587777756
Map	rs587777756
PheGenI	rs587777756
Biobank	rs587777756
1000 genomes	rs587777756
hgdp	rs587777756
ensembl	rs587777756
geneview	rs587777756
scholar	rs587777756
google	rs587777756
pharmgkb	rs587777756
gwascentral	rs587777756
openSNP	rs587777756
23andMe	rs587777756
SNPshot	rs587777756
SNPdbe	rs587777756
MSV3d	rs587777756
GWAS Ctlg	rs587777756

Max Magnitude

0

ClinVar
Risk	rs587777756(T;T)
Alt	rs587777756(T;T)
Reference	Rs587777756(-;-)
Significance	Pathogenic
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.32362039dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006021.2,