rs137852657

Orientation

plus

Stabilized

plus

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

Make rs137852657(C;T)

Make rs137852657(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

50591584

Gene

ATL1

is a	snp
is	mentioned by
dbSNP	rs137852657
dbSNP (classic)	rs137852657
ClinGen	rs137852657
ebi	rs137852657
HLI	rs137852657
Exac	rs137852657
Gnomad	rs137852657
Varsome	rs137852657
LitVar	rs137852657
Map	rs137852657
PheGenI	rs137852657
Biobank	rs137852657
1000 genomes	rs137852657
hgdp	rs137852657
ensembl	rs137852657
geneview	rs137852657
scholar	rs137852657
google	rs137852657
pharmgkb	rs137852657
gwascentral	rs137852657
openSNP	rs137852657
23andMe	rs137852657
SNPshot	rs137852657
SNPdbe	rs137852657
MSV3d	rs137852657
GWAS Ctlg	rs137852657

Max Magnitude

0

ClinVar
Risk	rs137852657(T;T)
Alt	rs137852657(T;T)
Reference	Rs137852657(C;C)
Significance	Pathogenic
Disease	Spastic paraplegia 3
Variation	info
Gene	ATL1
CLNDBN	Spastic paraplegia 3
Reversed	0
HGVS	NC_000014.8:g.51058302C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020721.2,