rs796052023

Orientation

plus

Stabilized

plus

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

Make rs796052023(-;-)

Make rs796052023(-;TGA)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

136316949

Gene

PCCB

is a	snp
is	mentioned by
dbSNP	rs796052023
dbSNP (classic)	rs796052023
ClinGen	rs796052023
ebi	rs796052023
HLI	rs796052023
Exac	rs796052023
Gnomad	rs796052023
Varsome	rs796052023
LitVar	rs796052023
Map	rs796052023
PheGenI	rs796052023
Biobank	rs796052023
1000 genomes	rs796052023
hgdp	rs796052023
ensembl	rs796052023
geneview	rs796052023
scholar	rs796052023
google	rs796052023
pharmgkb	rs796052023
gwascentral	rs796052023
openSNP	rs796052023
23andMe	rs796052023
SNPshot	rs796052023
SNPdbe	rs796052023
MSV3d	rs796052023
GWAS Ctlg	rs796052023

Max Magnitude

0

ClinVar
Risk	rs796052023(-;-)
Alt	rs796052023(-;-)
Reference	Rs796052023(TGA;TGA)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCCB
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.136035791_136035793delTGA
CLNSRC
CLNACC	RCV000186093.1,