rs72552771

Orientation

plus

Stabilized

plus

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

Make rs72552771(G;G)

Make rs72552771(G;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

75981072

Gene

POR

is a	snp
is	mentioned by
dbSNP	rs72552771
dbSNP (classic)	rs72552771
ClinGen	rs72552771
ebi	rs72552771
HLI	rs72552771
Exac	rs72552771
Gnomad	rs72552771
Varsome	rs72552771
LitVar	rs72552771
Map	rs72552771
PheGenI	rs72552771
Biobank	rs72552771
1000 genomes	rs72552771
hgdp	rs72552771
ensembl	rs72552771
geneview	rs72552771
scholar	rs72552771
google	rs72552771
pharmgkb	rs72552771
gwascentral	rs72552771
openSNP	rs72552771
23andMe	rs72552771
SNPshot	rs72552771
SNPdbe	rs72552771
MSV3d	rs72552771
GWAS Ctlg	rs72552771

Max Magnitude

0

OMIM	124015
Desc
Variant	0007
Related	also

ClinVar
Risk	rs72552771(G;G)
Alt	rs72552771(G;G)
Reference	Rs72552771(T;T)
Significance	Pathogenic
Disease	Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency
Variation	info
Gene	POR
CLNDBN	Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency
Reversed	0
HGVS	NC_000007.13:g.75610390T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018405.25,