rs776496862

Orientation

plus

Stabilized

plus

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

Make rs776496862(A;A)

Make rs776496862(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

100425674

Gene

PCCA

is a	snp
is	mentioned by
dbSNP	rs776496862
dbSNP (classic)	rs776496862
ClinGen	rs776496862
ebi	rs776496862
HLI	rs776496862
Exac	rs776496862
Gnomad	rs776496862
Varsome	rs776496862
LitVar	rs776496862
Map	rs776496862
PheGenI	rs776496862
Biobank	rs776496862
1000 genomes	rs776496862
hgdp	rs776496862
ensembl	rs776496862
geneview	rs776496862
scholar	rs776496862
google	rs776496862
pharmgkb	rs776496862
gwascentral	rs776496862
openSNP	rs776496862
23andMe	rs776496862
SNPshot	rs776496862
SNPdbe	rs776496862
MSV3d	rs776496862
GWAS Ctlg	rs776496862

Max Magnitude

0

ClinVar
Risk	rs776496862(A;A)
Alt	rs776496862(A;A)
Reference	Rs776496862(G;G)
Significance	Pathogenic
Disease	Propionic acidemia
Variation	info
Gene	PCCA
CLNDBN	Propionic acidemia
Reversed	0
HGVS	NC_000013.10:g.101077928G>A
CLNSRC
CLNACC	RCV000176030.1,