rs796052937

Orientation

plus

Stabilized

plus

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

Make rs796052937(A;T)

Make rs796052937(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

29814393

Gene	PAGR1, PRRT2

is a	snp
is	mentioned by
dbSNP	rs796052937
dbSNP (classic)	rs796052937
ClinGen	rs796052937
ebi	rs796052937
HLI	rs796052937
Exac	rs796052937
Gnomad	rs796052937
Varsome	rs796052937
LitVar	rs796052937
Map	rs796052937
PheGenI	rs796052937
Biobank	rs796052937
1000 genomes	rs796052937
hgdp	rs796052937
ensembl	rs796052937
geneview	rs796052937
scholar	rs796052937
google	rs796052937
pharmgkb	rs796052937
gwascentral	rs796052937
openSNP	rs796052937
23andMe	rs796052937
SNPshot	rs796052937
SNPdbe	rs796052937
MSV3d	rs796052937
GWAS Ctlg	rs796052937

Max Magnitude

0

ClinVar
Risk	rs796052937(T;T)
Alt	rs796052937(T;T)
Reference	Rs796052937(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PAGR1 PRRT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.29825714A>T
CLNSRC
CLNACC	RCV000188774.1,