rs797046006

Orientation

minus

Stabilized

minus

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

Make rs797046006(A;G)

Make rs797046006(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

66715958

Gene

SPTBN2

is a	snp
is	mentioned by
dbSNP	rs797046006
dbSNP (classic)	rs797046006
ClinGen	rs797046006
ebi	rs797046006
HLI	rs797046006
Exac	rs797046006
Gnomad	rs797046006
Varsome	rs797046006
LitVar	rs797046006
Map	rs797046006
PheGenI	rs797046006
Biobank	rs797046006
1000 genomes	rs797046006
hgdp	rs797046006
ensembl	rs797046006
geneview	rs797046006
scholar	rs797046006
google	rs797046006
pharmgkb	rs797046006
gwascentral	rs797046006
openSNP	rs797046006
23andMe	rs797046006
SNPshot	rs797046006
SNPdbe	rs797046006
MSV3d	rs797046006
GWAS Ctlg	rs797046006

Max Magnitude

0

ClinVar
Risk	rs797046006(G;G)
Alt	rs797046006(G;G)
Reference	Rs797046006(A;A)
Significance	Probable-Pathogenic
Disease	Ataxia not provided
Variation	info
Gene	SPTBN2
CLNDBN	Ataxia not provided
Reversed	1
HGVS	NC_000011.9:g.66483429T>C
CLNSRC
CLNACC	RCV000192407.1, RCV000494630.1,