rs1807467

Orientation

minus

Stabilized

minus

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

Make rs1807467(G;T)

Make rs1807467(T;T)

Reference

GRCh38 38.1/142

Chromosome

22

Position

18918380

Gene

PRODH

is a	snp
is	mentioned by
dbSNP	rs1807467
dbSNP (classic)	rs1807467
ClinGen	rs1807467
ebi	rs1807467
HLI	rs1807467
Exac	rs1807467
Gnomad	rs1807467
Varsome	rs1807467
LitVar	rs1807467
Map	rs1807467
PheGenI	rs1807467
Biobank	rs1807467
1000 genomes	rs1807467
hgdp	rs1807467
ensembl	rs1807467
geneview	rs1807467
scholar	rs1807467
google	rs1807467
pharmgkb	rs1807467
gwascentral	rs1807467
openSNP	rs1807467
23andMe	rs1807467
SNPshot	rs1807467
SNPdbe	rs1807467
MSV3d	rs1807467
GWAS Ctlg	rs1807467

Max Magnitude

0

OMIM	606810
Desc	HYPERPROLINEMIA, TYPE I
Variant	0005
Related	also

ClinVar
Risk	rs1807467(T;T)
Alt	rs1807467(T;T)
Reference	Rs1807467(G;G)
Significance	Other
Disease	Proline dehydrogenase deficiency Schizophrenia 4
Variation	info
Gene	PRODH
CLNDBN	Proline dehydrogenase deficiency Schizophrenia 4
Reversed	1
HGVS	NC_000022.10:g.18905893C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004220.6, RCV000004221.6,