rs1060502227

Orientation

plus

Stabilized

plus

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

Make rs1060502227(C;G)

Make rs1060502227(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

32136593

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs1060502227
dbSNP (classic)	rs1060502227
ClinGen	rs1060502227
ebi	rs1060502227
HLI	rs1060502227
Exac	rs1060502227
Gnomad	rs1060502227
Varsome	rs1060502227
LitVar	rs1060502227
Map	rs1060502227
PheGenI	rs1060502227
Biobank	rs1060502227
1000 genomes	rs1060502227
hgdp	rs1060502227
ensembl	rs1060502227
geneview	rs1060502227
scholar	rs1060502227
google	rs1060502227
pharmgkb	rs1060502227
gwascentral	rs1060502227
openSNP	rs1060502227
23andMe	rs1060502227
SNPshot	rs1060502227
SNPdbe	rs1060502227
MSV3d	rs1060502227
GWAS Ctlg	rs1060502227

Max Magnitude

0

ClinVar
Risk	rs1060502227(G;G)
Alt	rs1060502227(G;G)
Reference	Rs1060502227(C;C)
Significance	Pathogenic
Disease	Spastic paraplegia 4 not provided
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant not provided
Reversed	0
HGVS	NC_000002.11:g.32361662C>G
CLNSRC
CLNACC	RCV000459046.1, RCV000482415.1,