rs1057518880

Orientation

plus

Stabilized

plus

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

Make rs1057518880(-;-)

Make rs1057518880(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

32126966

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs1057518880
dbSNP (classic)	rs1057518880
ClinGen	rs1057518880
ebi	rs1057518880
HLI	rs1057518880
Exac	rs1057518880
Gnomad	rs1057518880
Varsome	rs1057518880
LitVar	rs1057518880
Map	rs1057518880
PheGenI	rs1057518880
Biobank	rs1057518880
1000 genomes	rs1057518880
hgdp	rs1057518880
ensembl	rs1057518880
geneview	rs1057518880
scholar	rs1057518880
google	rs1057518880
pharmgkb	rs1057518880
gwascentral	rs1057518880
openSNP	rs1057518880
23andMe	rs1057518880
SNPshot	rs1057518880
SNPdbe	rs1057518880
MSV3d	rs1057518880
GWAS Ctlg	rs1057518880

Max Magnitude

0

ClinVar
Risk	rs1057518880(-;-)
Alt	rs1057518880(-;-)
Reference	Rs1057518880(G;G)
Significance	Pathogenic
Disease	Spastic paraplegia
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia
Reversed	0
HGVS	NC_000002.11:g.32352035delG
CLNSRC
CLNACC	RCV000414756.1,