rs794727092

Orientation

plus

Stabilized

plus

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

Make rs794727092(G;T)

Make rs794727092(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

136327733

Gene

PCCB

is a	snp
is	mentioned by
dbSNP	rs794727092
dbSNP (classic)	rs794727092
ClinGen	rs794727092
ebi	rs794727092
HLI	rs794727092
Exac	rs794727092
Gnomad	rs794727092
Varsome	rs794727092
LitVar	rs794727092
Map	rs794727092
PheGenI	rs794727092
Biobank	rs794727092
1000 genomes	rs794727092
hgdp	rs794727092
ensembl	rs794727092
geneview	rs794727092
scholar	rs794727092
google	rs794727092
pharmgkb	rs794727092
gwascentral	rs794727092
openSNP	rs794727092
23andMe	rs794727092
SNPshot	rs794727092
SNPdbe	rs794727092
MSV3d	rs794727092
GWAS Ctlg	rs794727092

Max Magnitude

0

ClinVar
Risk	rs794727092(T;T)
Alt	rs794727092(T;T)
Reference	Rs794727092(G;G)
Significance	Pathogenic
Disease	Propionic acidemia
Variation	info
Gene	PCCB
CLNDBN	Propionic acidemia
Reversed	0
HGVS	NC_000003.11:g.136046575G>T
CLNSRC
CLNACC	RCV000174489.1,