rs1060501168

Orientation

minus

Stabilized

minus

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

Make rs1060501168(G;T)

Make rs1060501168(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

44575042

Gene

SPG11

is a	snp
is	mentioned by
dbSNP	rs1060501168
dbSNP (classic)	rs1060501168
ClinGen	rs1060501168
ebi	rs1060501168
HLI	rs1060501168
Exac	rs1060501168
Gnomad	rs1060501168
Varsome	rs1060501168
LitVar	rs1060501168
Map	rs1060501168
PheGenI	rs1060501168
Biobank	rs1060501168
1000 genomes	rs1060501168
hgdp	rs1060501168
ensembl	rs1060501168
geneview	rs1060501168
scholar	rs1060501168
google	rs1060501168
pharmgkb	rs1060501168
gwascentral	rs1060501168
openSNP	rs1060501168
23andMe	rs1060501168
SNPshot	rs1060501168
SNPdbe	rs1060501168
MSV3d	rs1060501168
GWAS Ctlg	rs1060501168

Max Magnitude

0

ClinVar
Risk	rs1060501168(T;T)
Alt	rs1060501168(T;T)
Reference	Rs1060501168(G;G)
Significance	Pathogenic
Disease	Spastic paraplegia 11
Variation	info
Gene	SPG11
CLNDBN	Spastic paraplegia 11, autosomal recessive
Reversed	1
HGVS	NC_000015.9:g.44867240C>A
CLNSRC
CLNACC	RCV000473393.1,