rs1060502226

Orientation

plus

Stabilized

plus

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

Make rs1060502226(A;A)

Make rs1060502226(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

32127023

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs1060502226
dbSNP (classic)	rs1060502226
ClinGen	rs1060502226
ebi	rs1060502226
HLI	rs1060502226
Exac	rs1060502226
Gnomad	rs1060502226
Varsome	rs1060502226
LitVar	rs1060502226
Map	rs1060502226
PheGenI	rs1060502226
Biobank	rs1060502226
1000 genomes	rs1060502226
hgdp	rs1060502226
ensembl	rs1060502226
geneview	rs1060502226
scholar	rs1060502226
google	rs1060502226
pharmgkb	rs1060502226
gwascentral	rs1060502226
openSNP	rs1060502226
23andMe	rs1060502226
SNPshot	rs1060502226
SNPdbe	rs1060502226
MSV3d	rs1060502226
GWAS Ctlg	rs1060502226

Max Magnitude

0

ClinVar
Risk	rs1060502226(A;A)
Alt	rs1060502226(A;A)
Reference	Rs1060502226(G;G)
Significance	Pathogenic
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.32352092G>A
CLNSRC
CLNACC	RCV000472388.1,