rs864622268

Orientation

plus

Stabilized

plus

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

Make rs864622268(-;-)

Make rs864622268(-;AG)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

32137132

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs864622268
dbSNP (classic)	rs864622268
ClinGen	rs864622268
ebi	rs864622268
HLI	rs864622268
Exac	rs864622268
Gnomad	rs864622268
Varsome	rs864622268
LitVar	rs864622268
Map	rs864622268
PheGenI	rs864622268
Biobank	rs864622268
1000 genomes	rs864622268
hgdp	rs864622268
ensembl	rs864622268
geneview	rs864622268
scholar	rs864622268
google	rs864622268
pharmgkb	rs864622268
gwascentral	rs864622268
openSNP	rs864622268
23andMe	rs864622268
SNPshot	rs864622268
SNPdbe	rs864622268
MSV3d	rs864622268
GWAS Ctlg	rs864622268

Max Magnitude

0

ClinVar
Risk	rs864622268(-;-)
Alt	rs864622268(-;-)
Reference	Rs864622268(AG;AG)
Significance	Pathogenic
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.32362201_32362202delAG
CLNSRC
CLNACC	RCV000204013.1,