rs777027944

Orientation

plus

Stabilized

plus

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

Make rs777027944(A;A)

Make rs777027944(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

136327166

Gene

PCCB

is a	snp
is	mentioned by
dbSNP	rs777027944
dbSNP (classic)	rs777027944
ClinGen	rs777027944
ebi	rs777027944
HLI	rs777027944
Exac	rs777027944
Gnomad	rs777027944
Varsome	rs777027944
LitVar	rs777027944
Map	rs777027944
PheGenI	rs777027944
Biobank	rs777027944
1000 genomes	rs777027944
hgdp	rs777027944
ensembl	rs777027944
geneview	rs777027944
scholar	rs777027944
google	rs777027944
pharmgkb	rs777027944
gwascentral	rs777027944
openSNP	rs777027944
23andMe	rs777027944
SNPshot	rs777027944
SNPdbe	rs777027944
MSV3d	rs777027944
GWAS Ctlg	rs777027944

Max Magnitude

0

ClinVar
Risk	rs777027944(A;A)
Alt	rs777027944(A;A)
Reference	Rs777027944(G;G)
Significance	Pathogenic
Disease	Propionic acidemia
Variation	info
Gene	PCCB
CLNDBN	Propionic acidemia
Reversed	0
HGVS	NC_000003.11:g.136046008G>A
CLNSRC
CLNACC	RCV000235547.1,