rs730882066

Orientation

plus

Stabilized

plus

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

Make rs730882066(-;-)

Make rs730882066(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

29814425

Gene	PAGR1, PRRT2

is a	snp
is	mentioned by
dbSNP	rs730882066
dbSNP (classic)	rs730882066
ClinGen	rs730882066
ebi	rs730882066
HLI	rs730882066
Exac	rs730882066
Gnomad	rs730882066
Varsome	rs730882066
LitVar	rs730882066
Map	rs730882066
PheGenI	rs730882066
Biobank	rs730882066
1000 genomes	rs730882066
hgdp	rs730882066
ensembl	rs730882066
geneview	rs730882066
scholar	rs730882066
google	rs730882066
pharmgkb	rs730882066
gwascentral	rs730882066
openSNP	rs730882066
23andMe	rs730882066
SNPshot	rs730882066
SNPdbe	rs730882066
MSV3d	rs730882066
GWAS Ctlg	rs730882066

Max Magnitude

0

ClinVar
Risk	rs730882066(-;-)
Alt	rs730882066(-;-)
Reference	Rs730882066(A;A)
Significance	Pathogenic
Disease	Dystonia 10
Variation	info
Gene	PAGR1 PRRT2
CLNDBN	Dystonia 10
Reversed	0
HGVS	NC_000016.9:g.29825746delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024168.4,