rs2870984

Orientation

plus

Stabilized

plus

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

Make rs2870984(A;A)

Make rs2870984(A;G)

Reference

GRCh38 38.1/141

Chromosome

22

Position

18918346

Gene

PRODH

is a	snp
is	mentioned by
dbSNP	rs2870984
dbSNP (classic)	rs2870984
ClinGen	rs2870984
ebi	rs2870984
HLI	rs2870984
Exac	rs2870984
Gnomad	rs2870984
Varsome	rs2870984
LitVar	rs2870984
Map	rs2870984
PheGenI	rs2870984
Biobank	rs2870984
1000 genomes	rs2870984
hgdp	rs2870984
ensembl	rs2870984
geneview	rs2870984
scholar	rs2870984
google	rs2870984
pharmgkb	rs2870984
gwascentral	rs2870984
openSNP	rs2870984
23andMe	rs2870984
SNPshot	rs2870984
SNPdbe	rs2870984
MSV3d	rs2870984
GWAS Ctlg	rs2870984

Max Magnitude

0

OMIM	606810
Desc	HYPERPROLINEMIA, TYPE I
Variant	0009
Related	also

ClinVar
Risk	rs2870984(A;A)
Alt	rs2870984(A;A)
Reference	Rs2870984(G;G)
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.18905859G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004227.8, RCV000004228.2,