rs796052018

Orientation

plus

Stabilized

plus

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

Make rs796052018(C;C)

Make rs796052018(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

100449297

Gene

PCCA

is a	snp
is	mentioned by
dbSNP	rs796052018
dbSNP (classic)	rs796052018
ClinGen	rs796052018
ebi	rs796052018
HLI	rs796052018
Exac	rs796052018
Gnomad	rs796052018
Varsome	rs796052018
LitVar	rs796052018
Map	rs796052018
PheGenI	rs796052018
Biobank	rs796052018
1000 genomes	rs796052018
hgdp	rs796052018
ensembl	rs796052018
geneview	rs796052018
scholar	rs796052018
google	rs796052018
pharmgkb	rs796052018
gwascentral	rs796052018
openSNP	rs796052018
23andMe	rs796052018
SNPshot	rs796052018
SNPdbe	rs796052018
MSV3d	rs796052018
GWAS Ctlg	rs796052018

Max Magnitude

0

ClinVar
Risk	rs796052018(C;C)
Alt	rs796052018(C;C)
Reference	Rs796052018(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCCA
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.101101551G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000186083.1,