rs778153326

Orientation

plus

Stabilized

plus

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

Make rs778153326(C;C)

Make rs778153326(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

12897789

Gene	GCDH, SYCE2

is a	snp
is	mentioned by
dbSNP	rs778153326
dbSNP (classic)	rs778153326
ClinGen	rs778153326
ebi	rs778153326
HLI	rs778153326
Exac	rs778153326
Gnomad	rs778153326
Varsome	rs778153326
LitVar	rs778153326
Map	rs778153326
PheGenI	rs778153326
Biobank	rs778153326
1000 genomes	rs778153326
hgdp	rs778153326
ensembl	rs778153326
geneview	rs778153326
scholar	rs778153326
google	rs778153326
pharmgkb	rs778153326
gwascentral	rs778153326
openSNP	rs778153326
23andMe	rs778153326
SNPshot	rs778153326
SNPdbe	rs778153326
MSV3d	rs778153326
GWAS Ctlg	rs778153326

Max Magnitude

0

ClinVar
Risk	rs778153326(C;C) rs778153326(T;T)
Alt	rs778153326(C;C) rs778153326(T;T)
Reference	Rs778153326(G;G)
Significance	Probable-Pathogenic
Disease	Glutaric aciduria
Variation	info
Gene	GCDH
CLNDBN	Glutaric aciduria, type 1
Reversed	0
HGVS	NC_000019.9:g.13008603G>C
CLNSRC
CLNACC	RCV000411911.1,