rs786205877

Merged into

rs10262966

Orientation

plus

Stabilized

plus

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

Make rs786205877(A;G)

Make rs786205877(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

75954007

Gene

POR

is a	snp
is	mentioned by
dbSNP	rs786205877
dbSNP (classic)	rs786205877
ClinGen	rs786205877
ebi	rs786205877
HLI	rs786205877
Exac	rs786205877
Gnomad	rs786205877
Varsome	rs786205877
LitVar	rs786205877
Map	rs786205877
PheGenI	rs786205877
Biobank	rs786205877
1000 genomes	rs786205877
hgdp	rs786205877
ensembl	rs786205877
geneview	rs786205877
scholar	rs786205877
google	rs786205877
pharmgkb	rs786205877
gwascentral	rs786205877
openSNP	rs786205877
23andMe	rs786205877
SNPshot	rs786205877
SNPdbe	rs786205877
MSV3d	rs786205877
GWAS Ctlg	rs786205877

Status

Merged into rs10262966

Max Magnitude

0

ClinVar
Risk	rs786205877(G;G)
Alt	rs786205877(G;G)
Reference	Rs786205877(A;A)
Significance	Pathogenic
Disease	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
Variation	info
Gene	POR
CLNDBN	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
Reversed	0
HGVS	NC_000007.14:g.75954007A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018413.27,