rs748309520

Orientation

plus

Stabilized

plus

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

Make rs748309520(A;A)

Make rs748309520(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

89531903

Gene

SPG7

is a	snp
is	mentioned by
dbSNP	rs748309520
dbSNP (classic)	rs748309520
ClinGen	rs748309520
ebi	rs748309520
HLI	rs748309520
Exac	rs748309520
Gnomad	rs748309520
Varsome	rs748309520
LitVar	rs748309520
Map	rs748309520
PheGenI	rs748309520
Biobank	rs748309520
1000 genomes	rs748309520
hgdp	rs748309520
ensembl	rs748309520
geneview	rs748309520
scholar	rs748309520
google	rs748309520
pharmgkb	rs748309520
gwascentral	rs748309520
openSNP	rs748309520
23andMe	rs748309520
SNPshot	rs748309520
SNPdbe	rs748309520
MSV3d	rs748309520
GWAS Ctlg	rs748309520

Max Magnitude

0

ClinVar
Risk	rs748309520(A;A)
Alt	rs748309520(A;A)
Reference	Rs748309520(G;G)
Significance	Other
Disease	Spastic paraplegia 7
Variation	info
Gene	SPG7
CLNDBN	Spastic paraplegia 7
Reversed	0
HGVS	NC_000016.9:g.89598311G>A
CLNSRC
CLNACC	RCV000206709.2,