rs886041735

Orientation

plus

Stabilized

plus

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

Chromosome

16

Position

29813261

Gene

PRRT2

is a	snp
is	mentioned by
dbSNP	rs886041735
dbSNP (classic)	rs886041735
ClinGen	rs886041735
ebi	rs886041735
HLI	rs886041735
Exac	rs886041735
Gnomad	rs886041735
Varsome	rs886041735
LitVar	rs886041735
Map	rs886041735
PheGenI	rs886041735
Biobank	rs886041735
1000 genomes	rs886041735
hgdp	rs886041735
ensembl	rs886041735
geneview	rs886041735
scholar	rs886041735
google	rs886041735
pharmgkb	rs886041735
gwascentral	rs886041735
openSNP	rs886041735
23andMe	rs886041735
SNPshot	rs886041735
SNPdbe	rs886041735
MSV3d	rs886041735
GWAS Ctlg	rs886041735

Max Magnitude

0

ClinVar
Risk	rs886041735(CCAAGGCTGGGCTGGCT;CCAAGGCTGGGCTGGCT)
Alt	rs886041735(CCAAGGCTGGGCTGGCT;CCAAGGCTGGGCTGGCT)
Reference	Rs886041735(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PRRT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.29824566_29824582dup17
CLNSRC
CLNACC	RCV000311228.1,