rs312262725

Orientation

minus

Stabilized

minus

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

Make rs312262725(-;A)

Make rs312262725(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

44651598

Gene

SPG11

is a	snp
is	mentioned by
dbSNP	rs312262725
dbSNP (classic)	rs312262725
ClinGen	rs312262725
ebi	rs312262725
HLI	rs312262725
Exac	rs312262725
Gnomad	rs312262725
Varsome	rs312262725
LitVar	rs312262725
Map	rs312262725
PheGenI	rs312262725
Biobank	rs312262725
1000 genomes	rs312262725
hgdp	rs312262725
ensembl	rs312262725
geneview	rs312262725
scholar	rs312262725
google	rs312262725
pharmgkb	rs312262725
gwascentral	rs312262725
openSNP	rs312262725
23andMe	rs312262725
SNPshot	rs312262725
SNPdbe	rs312262725
MSV3d	rs312262725
GWAS Ctlg	rs312262725

Max Magnitude

0

ClinVar
Risk	rs312262725(A;A)
Alt	rs312262725(A;A)
Reference	Rs312262725(-;-)
Significance	Pathogenic
Disease	Spastic paraplegia 11
Variation	info
Gene	SPG11
CLNDBN	Spastic paraplegia 11, autosomal recessive
Reversed	1
HGVS	NC_000015.9:g.44943797dupT
CLNSRC
CLNACC	RCV000227208.1,