rs796052936

Orientation

plus

Stabilized

plus

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

Make rs796052936(A;A)

Make rs796052936(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

29813926

Gene

PRRT2

is a	snp
is	mentioned by
dbSNP	rs796052936
dbSNP (classic)	rs796052936
ClinGen	rs796052936
ebi	rs796052936
HLI	rs796052936
Exac	rs796052936
Gnomad	rs796052936
Varsome	rs796052936
LitVar	rs796052936
Map	rs796052936
PheGenI	rs796052936
Biobank	rs796052936
1000 genomes	rs796052936
hgdp	rs796052936
ensembl	rs796052936
geneview	rs796052936
scholar	rs796052936
google	rs796052936
pharmgkb	rs796052936
gwascentral	rs796052936
openSNP	rs796052936
23andMe	rs796052936
SNPshot	rs796052936
SNPdbe	rs796052936
MSV3d	rs796052936
GWAS Ctlg	rs796052936

Max Magnitude

0

ClinVar
Risk	rs796052936(A;A)
Alt	rs796052936(A;A)
Reference	Rs796052936(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC100289283 PRRT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.29825247C>A
CLNSRC
CLNACC	RCV000188772.2,