rs2904552

Orientation

plus

Stabilized

plus

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

Make rs2904552(C;T)

Make rs2904552(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

18918451

Gene

PRODH

is a	snp
is	mentioned by
dbSNP	rs2904552
dbSNP (classic)	rs2904552
ClinGen	rs2904552
ebi	rs2904552
HLI	rs2904552
Exac	rs2904552
Gnomad	rs2904552
Varsome	rs2904552
LitVar	rs2904552
Map	rs2904552
PheGenI	rs2904552
Biobank	rs2904552
1000 genomes	rs2904552
hgdp	rs2904552
ensembl	rs2904552
geneview	rs2904552
scholar	rs2904552
google	rs2904552
pharmgkb	rs2904552
gwascentral	rs2904552
openSNP	rs2904552
23andMe	rs2904552
SNPshot	rs2904552
SNPdbe	rs2904552
MSV3d	rs2904552
GWAS Ctlg	rs2904552

GMAF

0.05005

Max Magnitude

0

OMIM	606810
Desc	HYPERPROLINEMIA, TYPE I
Variant	0007
Related	also

ClinVar
Risk	rs2904552(T;T)
Alt	rs2904552(T;T)
Reference	Rs2904552(C;C)
Significance	Other
Disease	Proline dehydrogenase deficiency Schizophrenia 4
Variation	info
Gene	PRODH
CLNDBN	Proline dehydrogenase deficiency Schizophrenia 4
Reversed	0
HGVS	NC_000022.10:g.18905964C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004224.5, RCV000004225.5,