rs796052944

Orientation

plus

Stabilized

plus

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

Make rs796052944(-;C)

Make rs796052944(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

29813487

Gene

PRRT2

is a	snp
is	mentioned by
dbSNP	rs796052944
dbSNP (classic)	rs796052944
ClinGen	rs796052944
ebi	rs796052944
HLI	rs796052944
Exac	rs796052944
Gnomad	rs796052944
Varsome	rs796052944
LitVar	rs796052944
Map	rs796052944
PheGenI	rs796052944
Biobank	rs796052944
1000 genomes	rs796052944
hgdp	rs796052944
ensembl	rs796052944
geneview	rs796052944
scholar	rs796052944
google	rs796052944
pharmgkb	rs796052944
gwascentral	rs796052944
openSNP	rs796052944
23andMe	rs796052944
SNPshot	rs796052944
SNPdbe	rs796052944
MSV3d	rs796052944
GWAS Ctlg	rs796052944

Max Magnitude

0

ClinVar
Risk	rs796052944(C;C)
Alt	rs796052944(C;C)
Reference	Rs796052944(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LOC100289283 PRRT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.29824808dupC
CLNSRC
CLNACC	RCV000188785.1,