rs76335820

Orientation

plus

Stabilized

plus

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

Make rs76335820(C;T)

Make rs76335820(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

29813701

Gene

PRRT2

is a	snp
is	mentioned by
dbSNP	rs76335820
dbSNP (classic)	rs76335820
ClinGen	rs76335820
ebi	rs76335820
HLI	rs76335820
Exac	rs76335820
Gnomad	rs76335820
Varsome	rs76335820
LitVar	rs76335820
Map	rs76335820
PheGenI	rs76335820
Biobank	rs76335820
1000 genomes	rs76335820
hgdp	rs76335820
ensembl	rs76335820
geneview	rs76335820
scholar	rs76335820
google	rs76335820
pharmgkb	rs76335820
gwascentral	rs76335820
openSNP	rs76335820
23andMe	rs76335820
SNPshot	rs76335820
SNPdbe	rs76335820
MSV3d	rs76335820
GWAS Ctlg	rs76335820

Max Magnitude

0

ClinVar
Risk	rs76335820(A;A) rs76335820(G;G) rs76335820(T;T)
Alt	rs76335820(A;A) rs76335820(G;G) rs76335820(T;T)
Reference	Rs76335820(C;C)
Significance	Other
Disease	not specified Dystonia 10 not provided
Variation	info
Gene	LOC100289283 PRRT2
CLNDBN	not specified Dystonia 10 not provided
Reversed	0
HGVS	NC_000016.9:g.29825022C>A; NC_000016.9:g.29825022C>G; NC_000016.9:g.29825022C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000188770.2, RCV000229187.2, RCV000055990.1, RCV000188771.3, RCV000082646.8, RCV000224146.1, RCV000233107.2,