rs786204163

Orientation

plus

Stabilized

plus

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

Make rs786204163(C;C)

Make rs786204163(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

32137108

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs786204163
dbSNP (classic)	rs786204163
ClinGen	rs786204163
ebi	rs786204163
HLI	rs786204163
Exac	rs786204163
Gnomad	rs786204163
Varsome	rs786204163
LitVar	rs786204163
Map	rs786204163
PheGenI	rs786204163
Biobank	rs786204163
1000 genomes	rs786204163
hgdp	rs786204163
ensembl	rs786204163
geneview	rs786204163
scholar	rs786204163
google	rs786204163
pharmgkb	rs786204163
gwascentral	rs786204163
openSNP	rs786204163
23andMe	rs786204163
SNPshot	rs786204163
SNPdbe	rs786204163
MSV3d	rs786204163
GWAS Ctlg	rs786204163

Max Magnitude

0

ClinVar
Risk	rs786204163(C;C)
Alt	rs786204163(C;C)
Reference	Rs786204163(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.32362177G>C
CLNSRC
CLNACC	RCV000168164.1,