rs121908510

Orientation

plus

Stabilized

plus

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

Make rs121908510(A;A)

Make rs121908510(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

32136898

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs121908510
dbSNP (classic)	rs121908510
ClinGen	rs121908510
ebi	rs121908510
HLI	rs121908510
Exac	rs121908510
Gnomad	rs121908510
Varsome	rs121908510
LitVar	rs121908510
Map	rs121908510
PheGenI	rs121908510
Biobank	rs121908510
1000 genomes	rs121908510
hgdp	rs121908510
ensembl	rs121908510
geneview	rs121908510
scholar	rs121908510
google	rs121908510
pharmgkb	rs121908510
gwascentral	rs121908510
openSNP	rs121908510
23andMe	rs121908510
SNPshot	rs121908510
SNPdbe	rs121908510
MSV3d	rs121908510
GWAS Ctlg	rs121908510

Max Magnitude

0

OMIM	604277
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908510(A;A)
Alt	rs121908510(A;A)
Reference	Rs121908510(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.32361967G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006012.2,