rs796052020

Orientation

plus

Stabilized

plus

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

Make rs796052020(A;G)

Make rs796052020(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

136293754

Gene

PCCB

is a	snp
is	mentioned by
dbSNP	rs796052020
dbSNP (classic)	rs796052020
ClinGen	rs796052020
ebi	rs796052020
HLI	rs796052020
Exac	rs796052020
Gnomad	rs796052020
Varsome	rs796052020
LitVar	rs796052020
Map	rs796052020
PheGenI	rs796052020
Biobank	rs796052020
1000 genomes	rs796052020
hgdp	rs796052020
ensembl	rs796052020
geneview	rs796052020
scholar	rs796052020
google	rs796052020
pharmgkb	rs796052020
gwascentral	rs796052020
openSNP	rs796052020
23andMe	rs796052020
SNPshot	rs796052020
SNPdbe	rs796052020
MSV3d	rs796052020
GWAS Ctlg	rs796052020

Max Magnitude

0

ClinVar
Risk	rs796052020(G;G)
Alt	rs796052020(G;G)
Reference	Rs796052020(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCCB
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.136012596A>G
CLNSRC
CLNACC	RCV000186086.1,