rs796052025

Orientation

plus

Stabilized

plus

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

Make rs796052025(G;T)

Make rs796052025(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

136255931

Gene

PCCB

is a	snp
is	mentioned by
dbSNP	rs796052025
dbSNP (classic)	rs796052025
ClinGen	rs796052025
ebi	rs796052025
HLI	rs796052025
Exac	rs796052025
Gnomad	rs796052025
Varsome	rs796052025
LitVar	rs796052025
Map	rs796052025
PheGenI	rs796052025
Biobank	rs796052025
1000 genomes	rs796052025
hgdp	rs796052025
ensembl	rs796052025
geneview	rs796052025
scholar	rs796052025
google	rs796052025
pharmgkb	rs796052025
gwascentral	rs796052025
openSNP	rs796052025
23andMe	rs796052025
SNPshot	rs796052025
SNPdbe	rs796052025
MSV3d	rs796052025
GWAS Ctlg	rs796052025

Max Magnitude

0

ClinVar
Risk	rs796052025(T;T)
Alt	rs796052025(T;T)
Reference	Rs796052025(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCCB
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.135974773G>T
CLNSRC
CLNACC	RCV000186097.1,