rs121434372

Orientation

plus

Stabilized

plus

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

Make rs121434372(A;A)

Make rs121434372(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

12897818

Gene	GCDH, SYCE2

is a	snp
is	mentioned by
dbSNP	rs121434372
dbSNP (classic)	rs121434372
ClinGen	rs121434372
ebi	rs121434372
HLI	rs121434372
Exac	rs121434372
Gnomad	rs121434372
Varsome	rs121434372
LitVar	rs121434372
Map	rs121434372
PheGenI	rs121434372
Biobank	rs121434372
1000 genomes	rs121434372
hgdp	rs121434372
ensembl	rs121434372
geneview	rs121434372
scholar	rs121434372
google	rs121434372
pharmgkb	rs121434372
gwascentral	rs121434372
openSNP	rs121434372
23andMe	rs121434372
SNPshot	rs121434372
SNPdbe	rs121434372
MSV3d	rs121434372
GWAS Ctlg	rs121434372

Max Magnitude

0

OMIM	608801
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121434372(A;A)
Alt	rs121434372(A;A)
Reference	Rs121434372(G;G)
Significance	Pathogenic
Disease	Glutaric aciduria not provided
Variation	info
Gene	GCDH
CLNDBN	Glutaric aciduria, type 1 not provided
Reversed	0
HGVS	NC_000019.9:g.13008632G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002169.2, RCV000224327.2,