rs397515475

Orientation

minus

Stabilized

minus

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

Make rs397515475(-;-)

Make rs397515475(-;TCT)

Reference

GRCh38 38.1/141

Chromosome

1

Position

111982045

Gene

KCND3

is a	snp
is	mentioned by
dbSNP	rs397515475
dbSNP (classic)	rs397515475
ClinGen	rs397515475
ebi	rs397515475
HLI	rs397515475
Exac	rs397515475
Gnomad	rs397515475
Varsome	rs397515475
LitVar	rs397515475
Map	rs397515475
PheGenI	rs397515475
Biobank	rs397515475
1000 genomes	rs397515475
hgdp	rs397515475
ensembl	rs397515475
geneview	rs397515475
scholar	rs397515475
google	rs397515475
pharmgkb	rs397515475
gwascentral	rs397515475
openSNP	rs397515475
23andMe	rs397515475
SNPshot	rs397515475
SNPdbe	rs397515475
MSV3d	rs397515475
GWAS Ctlg	rs397515475

Max Magnitude

0

ClinVar
Risk	rs397515475(-;-)
Alt	rs397515475(-;-)
Reference	Rs397515475(TCT;TCT)
Significance	Pathogenic
Disease	Spinocerebellar ataxia 19
Variation	info
Gene	KCND3
CLNDBN	Spinocerebellar ataxia 19
Reversed	1
HGVS	NC_000001.10:g.112524667_112524669delAGA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000056298.3,