rs786205229

Orientation

minus

Stabilized

minus

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

Make rs786205229(C;T)

Make rs786205229(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

85543737

Gene

SNX14

is a	snp
is	mentioned by
dbSNP	rs786205229
dbSNP (classic)	rs786205229
ClinGen	rs786205229
ebi	rs786205229
HLI	rs786205229
Exac	rs786205229
Gnomad	rs786205229
Varsome	rs786205229
LitVar	rs786205229
Map	rs786205229
PheGenI	rs786205229
Biobank	rs786205229
1000 genomes	rs786205229
hgdp	rs786205229
ensembl	rs786205229
geneview	rs786205229
scholar	rs786205229
google	rs786205229
pharmgkb	rs786205229
gwascentral	rs786205229
openSNP	rs786205229
23andMe	rs786205229
SNPshot	rs786205229
SNPdbe	rs786205229
MSV3d	rs786205229
GWAS Ctlg	rs786205229

Max Magnitude

0

ClinVar
Risk	rs786205229(T;T)
Alt	rs786205229(T;T)
Reference	Rs786205229(C;C)
Significance	Pathogenic
Disease	Spinocerebellar ataxia
Variation	info
Gene	SNX14
CLNDBN	Spinocerebellar ataxia, autosomal recessive 20
Reversed	1
HGVS	NC_000006.11:g.86253455G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000170506.3,