rs1060499670

Orientation

plus

Stabilized

plus

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

Make rs1060499670(C;T)

Make rs1060499670(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

32126960

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs1060499670
dbSNP (classic)	rs1060499670
ClinGen	rs1060499670
ebi	rs1060499670
HLI	rs1060499670
Exac	rs1060499670
Gnomad	rs1060499670
Varsome	rs1060499670
LitVar	rs1060499670
Map	rs1060499670
PheGenI	rs1060499670
Biobank	rs1060499670
1000 genomes	rs1060499670
hgdp	rs1060499670
ensembl	rs1060499670
geneview	rs1060499670
scholar	rs1060499670
google	rs1060499670
pharmgkb	rs1060499670
gwascentral	rs1060499670
openSNP	rs1060499670
23andMe	rs1060499670
SNPshot	rs1060499670
SNPdbe	rs1060499670
MSV3d	rs1060499670
GWAS Ctlg	rs1060499670

Max Magnitude

0

ClinVar
Risk	rs1060499670(T;T)
Alt	rs1060499670(T;T)
Reference	Rs1060499670(C;C)
Significance	Probable-Pathogenic
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.32352029C>T
CLNSRC
CLNACC	RCV000449607.1,