rs397515576

Orientation

plus

Stabilized

plus

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

Make rs397515576(-;T)

Make rs397515576(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

29813564

Gene

PRRT2

is a	snp
is	mentioned by
dbSNP	rs397515576
dbSNP (classic)	rs397515576
ClinGen	rs397515576
ebi	rs397515576
HLI	rs397515576
Exac	rs397515576
Gnomad	rs397515576
Varsome	rs397515576
LitVar	rs397515576
Map	rs397515576
PheGenI	rs397515576
Biobank	rs397515576
1000 genomes	rs397515576
hgdp	rs397515576
ensembl	rs397515576
geneview	rs397515576
scholar	rs397515576
google	rs397515576
pharmgkb	rs397515576
gwascentral	rs397515576
openSNP	rs397515576
23andMe	rs397515576
SNPshot	rs397515576
SNPdbe	rs397515576
MSV3d	rs397515576
GWAS Ctlg	rs397515576

Max Magnitude

0

ClinVar
Risk	rs397515576(T;T)
Alt	rs397515576(T;T)
Reference	Rs397515576(-;-)
Significance	Pathogenic
Disease	Dystonia 10
Variation	info
Gene	LOC100289283 PRRT2
CLNDBN	Dystonia 10
Reversed	0
HGVS	NC_000016.9:g.29824885dupT
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055989.1,