rs864321669

Orientation

minus

Stabilized

minus

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

Make rs864321669(C;C)

Make rs864321669(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

95633040

Gene

ALDH18A1

is a	snp
is	mentioned by
dbSNP	rs864321669
dbSNP (classic)	rs864321669
ClinGen	rs864321669
ebi	rs864321669
HLI	rs864321669
Exac	rs864321669
Gnomad	rs864321669
Varsome	rs864321669
LitVar	rs864321669
Map	rs864321669
PheGenI	rs864321669
Biobank	rs864321669
1000 genomes	rs864321669
hgdp	rs864321669
ensembl	rs864321669
geneview	rs864321669
scholar	rs864321669
google	rs864321669
pharmgkb	rs864321669
gwascentral	rs864321669
openSNP	rs864321669
23andMe	rs864321669
SNPshot	rs864321669
SNPdbe	rs864321669
MSV3d	rs864321669
GWAS Ctlg	rs864321669

Max Magnitude

0

ClinVar
Risk	rs864321669(C;C)
Alt	rs864321669(C;C)
Reference	Rs864321669(G;G)
Significance	Pathogenic
Disease	Spastic paraplegia 9
Variation	info
Gene	ALDH18A1
CLNDBN	Spastic paraplegia 9
Reversed	1
HGVS	NC_000010.10:g.97392797C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000200956.2,