rs875989878

Orientation

plus

Stabilized

plus

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

Make rs875989878(A;A)

Make rs875989878(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

32128480

Gene

SPAST

is a	snp
is	mentioned by
dbSNP	rs875989878
dbSNP (classic)	rs875989878
ClinGen	rs875989878
ebi	rs875989878
HLI	rs875989878
Exac	rs875989878
Gnomad	rs875989878
Varsome	rs875989878
LitVar	rs875989878
Map	rs875989878
PheGenI	rs875989878
Biobank	rs875989878
1000 genomes	rs875989878
hgdp	rs875989878
ensembl	rs875989878
geneview	rs875989878
scholar	rs875989878
google	rs875989878
pharmgkb	rs875989878
gwascentral	rs875989878
openSNP	rs875989878
23andMe	rs875989878
SNPshot	rs875989878
SNPdbe	rs875989878
MSV3d	rs875989878
GWAS Ctlg	rs875989878

Max Magnitude

0

ClinVar
Risk	rs875989878(A;A)
Alt	rs875989878(A;A)
Reference	Rs875989878(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.32353549G>A
CLNSRC
CLNACC	RCV000211536.1,