rs796052938

Orientation

plus

Stabilized

plus

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

Make rs796052938(C;C)

Make rs796052938(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

29814424

Gene	PAGR1, PRRT2

is a	snp
is	mentioned by
dbSNP	rs796052938
dbSNP (classic)	rs796052938
ClinGen	rs796052938
ebi	rs796052938
HLI	rs796052938
Exac	rs796052938
Gnomad	rs796052938
Varsome	rs796052938
LitVar	rs796052938
Map	rs796052938
PheGenI	rs796052938
Biobank	rs796052938
1000 genomes	rs796052938
hgdp	rs796052938
ensembl	rs796052938
geneview	rs796052938
scholar	rs796052938
google	rs796052938
pharmgkb	rs796052938
gwascentral	rs796052938
openSNP	rs796052938
23andMe	rs796052938
SNPshot	rs796052938
SNPdbe	rs796052938
MSV3d	rs796052938
GWAS Ctlg	rs796052938

Max Magnitude

0

ClinVar
Risk	rs796052938(C;C)
Alt	rs796052938(C;C)
Reference	Rs796052938(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PAGR1 PRRT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.29825745G>C
CLNSRC
CLNACC	RCV000188775.2,