rs1057518873

Orientation

plus

Stabilized

plus

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

Make rs1057518873(C;G)

Make rs1057518873(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

32144990

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs1057518873
dbSNP (classic)	rs1057518873
ClinGen	rs1057518873
ebi	rs1057518873
HLI	rs1057518873
Exac	rs1057518873
Gnomad	rs1057518873
Varsome	rs1057518873
LitVar	rs1057518873
Map	rs1057518873
PheGenI	rs1057518873
Biobank	rs1057518873
1000 genomes	rs1057518873
hgdp	rs1057518873
ensembl	rs1057518873
geneview	rs1057518873
scholar	rs1057518873
google	rs1057518873
pharmgkb	rs1057518873
gwascentral	rs1057518873
openSNP	rs1057518873
23andMe	rs1057518873
SNPshot	rs1057518873
SNPdbe	rs1057518873
MSV3d	rs1057518873
GWAS Ctlg	rs1057518873

Max Magnitude

0

ClinVar
Risk	rs1057518873(G;G)
Alt	rs1057518873(G;G)
Reference	Rs1057518873(C;C)
Significance	Probable-Pathogenic
Disease	Spastic paraparesis
Variation	info
Gene	SPAST
CLNDBN	Spastic paraparesis
Reversed	0
HGVS	NC_000002.11:g.32370059C>G
CLNSRC
CLNACC	RCV000415025.1,