rs202247820

Orientation

plus

Stabilized

plus

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

Make rs202247820(C;T)

Make rs202247820(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

136328854

Gene

PCCB

is a	snp
is	mentioned by
dbSNP	rs202247820
dbSNP (classic)	rs202247820
ClinGen	rs202247820
ebi	rs202247820
HLI	rs202247820
Exac	rs202247820
Gnomad	rs202247820
Varsome	rs202247820
LitVar	rs202247820
Map	rs202247820
PheGenI	rs202247820
Biobank	rs202247820
1000 genomes	rs202247820
hgdp	rs202247820
ensembl	rs202247820
geneview	rs202247820
scholar	rs202247820
google	rs202247820
pharmgkb	rs202247820
gwascentral	rs202247820
openSNP	rs202247820
23andMe	rs202247820
SNPshot	rs202247820
SNPdbe	rs202247820
MSV3d	rs202247820
GWAS Ctlg	rs202247820

Max Magnitude

0

ClinVar
Risk	rs202247820(T;T)
Alt	rs202247820(T;T)
Reference	Rs202247820(C;C)
Significance	Pathogenic
Disease	Propionic acidemia
Variation	info
Gene	PCCB
CLNDBN	Propionic acidemia
Reversed	0
HGVS	NC_000003.11:g.136047696C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000032127.1,