rs886037833

Orientation

minus

Stabilized

minus

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

Make rs886037833(C;C)

Make rs886037833(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

11

Position

6616361

Gene

TPP1

is a	snp
is	mentioned by
dbSNP	rs886037833
dbSNP (classic)	rs886037833
ClinGen	rs886037833
ebi	rs886037833
HLI	rs886037833
Exac	rs886037833
Gnomad	rs886037833
Varsome	rs886037833
LitVar	rs886037833
Map	rs886037833
PheGenI	rs886037833
Biobank	rs886037833
1000 genomes	rs886037833
hgdp	rs886037833
ensembl	rs886037833
geneview	rs886037833
scholar	rs886037833
google	rs886037833
pharmgkb	rs886037833
gwascentral	rs886037833
openSNP	rs886037833
23andMe	rs886037833
SNPshot	rs886037833
SNPdbe	rs886037833
MSV3d	rs886037833
GWAS Ctlg	rs886037833

Max Magnitude

0

ClinVar
Risk	rs886037833(C;C)
Alt	rs886037833(C;C)
Reference	Rs886037833(G;G)
Significance	Pathogenic
Disease	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
Variation	info
Gene	TPP1
CLNDBN	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
Reversed	1
HGVS	NC_000011.9:g.6637592C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000211004.1,