rs121908516

Orientation

plus

Stabilized

plus

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

Make rs121908516(A;T)

Make rs121908516(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

32136964

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs121908516
dbSNP (classic)	rs121908516
ClinGen	rs121908516
ebi	rs121908516
HLI	rs121908516
Exac	rs121908516
Gnomad	rs121908516
Varsome	rs121908516
LitVar	rs121908516
Map	rs121908516
PheGenI	rs121908516
Biobank	rs121908516
1000 genomes	rs121908516
hgdp	rs121908516
ensembl	rs121908516
geneview	rs121908516
scholar	rs121908516
google	rs121908516
pharmgkb	rs121908516
gwascentral	rs121908516
openSNP	rs121908516
23andMe	rs121908516
SNPshot	rs121908516
SNPdbe	rs121908516
MSV3d	rs121908516
GWAS Ctlg	rs121908516

Merged from

Rs28939368

Max Magnitude

0

OMIM	604277
Desc
Variant	0016
Related	also

ClinVar
Risk	rs121908516(T;T)
Alt	rs121908516(T;T)
Reference	Rs121908516(A;A)
Significance	Pathogenic
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.32362033A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006024.2,