rs796052941

Orientation

plus

Stabilized

plus

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

Make rs796052941(-;-)

Make rs796052941(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

29814424

Gene	PAGR1, PRRT2

is a	snp
is	mentioned by
dbSNP	rs796052941
dbSNP (classic)	rs796052941
ClinGen	rs796052941
ebi	rs796052941
HLI	rs796052941
Exac	rs796052941
Gnomad	rs796052941
Varsome	rs796052941
LitVar	rs796052941
Map	rs796052941
PheGenI	rs796052941
Biobank	rs796052941
1000 genomes	rs796052941
hgdp	rs796052941
ensembl	rs796052941
geneview	rs796052941
scholar	rs796052941
google	rs796052941
pharmgkb	rs796052941
gwascentral	rs796052941
openSNP	rs796052941
23andMe	rs796052941
SNPshot	rs796052941
SNPdbe	rs796052941
MSV3d	rs796052941
GWAS Ctlg	rs796052941

Max Magnitude

0

ClinVar
Risk	rs796052941(-;-)
Alt	rs796052941(-;-)
Reference	Rs796052941(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PAGR1 PRRT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.29825745delG
CLNSRC
CLNACC	RCV000188780.2,