rs797045006

Orientation

minus

Stabilized

minus

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

Make rs797045006(A;A)

Make rs797045006(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

42850904

Gene

RNF170

is a	snp
is	mentioned by
dbSNP	rs797045006
dbSNP (classic)	rs797045006
ClinGen	rs797045006
ebi	rs797045006
HLI	rs797045006
Exac	rs797045006
Gnomad	rs797045006
Varsome	rs797045006
LitVar	rs797045006
Map	rs797045006
PheGenI	rs797045006
Biobank	rs797045006
1000 genomes	rs797045006
hgdp	rs797045006
ensembl	rs797045006
geneview	rs797045006
scholar	rs797045006
google	rs797045006
pharmgkb	rs797045006
gwascentral	rs797045006
openSNP	rs797045006
23andMe	rs797045006
SNPshot	rs797045006
SNPdbe	rs797045006
MSV3d	rs797045006
GWAS Ctlg	rs797045006

Max Magnitude

0

ClinVar
Risk	rs797045006(A;A)
Alt	rs797045006(A;A)
Reference	Rs797045006(G;G)
Significance	Probable-Pathogenic
Disease	Ataxia
Variation	info
Gene	RNF170
CLNDBN	Ataxia, sensory, autosomal dominant
Reversed	1
HGVS	NC_000008.10:g.42706047C>T
CLNSRC
CLNACC	RCV000190504.2,