rs121908517

Orientation

plus

Stabilized

plus

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

Make rs121908517(A;A)

Make rs121908517(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

32063965

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs121908517
dbSNP (classic)	rs121908517
ClinGen	rs121908517
ebi	rs121908517
HLI	rs121908517
Exac	rs121908517
Gnomad	rs121908517
Varsome	rs121908517
LitVar	rs121908517
Map	rs121908517
PheGenI	rs121908517
Biobank	rs121908517
1000 genomes	rs121908517
hgdp	rs121908517
ensembl	rs121908517
geneview	rs121908517
scholar	rs121908517
google	rs121908517
pharmgkb	rs121908517
gwascentral	rs121908517
openSNP	rs121908517
23andMe	rs121908517
SNPshot	rs121908517
SNPdbe	rs121908517
MSV3d	rs121908517
GWAS Ctlg	rs121908517

Max Magnitude

0

OMIM	604277
Desc
Variant	0017
Related	also

ClinVar
Risk	rs121908517(A;A)
Alt	rs121908517(A;A)
Reference	Rs121908517(C;C)
Significance	Other
Disease	Spastic paraplegia 4
Variation	info
Gene	SPAST
CLNDBN	Spastic paraplegia 4, modifier of
Reversed	0
HGVS	NC_000002.11:g.32289034C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006026.3,