rs796052940

Orientation

plus

Stabilized

plus

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

Make rs796052940(-;-)

Make rs796052940(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

29813227

Gene

PRRT2

is a	snp
is	mentioned by
dbSNP	rs796052940
dbSNP (classic)	rs796052940
ClinGen	rs796052940
ebi	rs796052940
HLI	rs796052940
Exac	rs796052940
Gnomad	rs796052940
Varsome	rs796052940
LitVar	rs796052940
Map	rs796052940
PheGenI	rs796052940
Biobank	rs796052940
1000 genomes	rs796052940
hgdp	rs796052940
ensembl	rs796052940
geneview	rs796052940
scholar	rs796052940
google	rs796052940
pharmgkb	rs796052940
gwascentral	rs796052940
openSNP	rs796052940
23andMe	rs796052940
SNPshot	rs796052940
SNPdbe	rs796052940
MSV3d	rs796052940
GWAS Ctlg	rs796052940

Max Magnitude

0

ClinVar
Risk	rs796052940(-;-)
Alt	rs796052940(-;-)
Reference	Rs796052940(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LOC100289283 PRRT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.29824548delC
CLNSRC
CLNACC	RCV000188777.1,