rs151344517

Orientation

minus

Stabilized

minus

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

Make rs151344517(A;A)

Make rs151344517(A;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

12337505

Gene	AFG3L2, LOC107985154

is a	snp
is	mentioned by
dbSNP	rs151344517
dbSNP (classic)	rs151344517
ClinGen	rs151344517
ebi	rs151344517
HLI	rs151344517
Exac	rs151344517
Gnomad	rs151344517
Varsome	rs151344517
LitVar	rs151344517
Map	rs151344517
PheGenI	rs151344517
Biobank	rs151344517
1000 genomes	rs151344517
hgdp	rs151344517
ensembl	rs151344517
geneview	rs151344517
scholar	rs151344517
google	rs151344517
pharmgkb	rs151344517
gwascentral	rs151344517
openSNP	rs151344517
23andMe	rs151344517
SNPshot	rs151344517
SNPdbe	rs151344517
MSV3d	rs151344517
GWAS Ctlg	rs151344517

Max Magnitude

0

ClinVar
Risk	rs151344517(A;A)
Alt	rs151344517(A;A)
Reference	Rs151344517(G;G)
Significance	Pathogenic
Disease	Spinocerebellar ataxia 28
Variation	info
Gene	AFG3L2
CLNDBN	Spinocerebellar ataxia 28
Reversed	1
HGVS	NC_000018.9:g.12337504C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023378.3,