rs886039769

Orientation

minus

Stabilized

minus

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

Make rs886039769(C;T)

Make rs886039769(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

124500686

Gene

NR5A1

is a	snp
is	mentioned by
dbSNP	rs886039769
dbSNP (classic)	rs886039769
ClinGen	rs886039769
ebi	rs886039769
HLI	rs886039769
Exac	rs886039769
Gnomad	rs886039769
Varsome	rs886039769
LitVar	rs886039769
Map	rs886039769
PheGenI	rs886039769
Biobank	rs886039769
1000 genomes	rs886039769
hgdp	rs886039769
ensembl	rs886039769
geneview	rs886039769
scholar	rs886039769
google	rs886039769
pharmgkb	rs886039769
gwascentral	rs886039769
openSNP	rs886039769
23andMe	rs886039769
SNPshot	rs886039769
SNPdbe	rs886039769
MSV3d	rs886039769
GWAS Ctlg	rs886039769

Max Magnitude

0

ClinVar
Risk	rs886039769(T;T)
Alt	rs886039769(T;T)
Reference	Rs886039769(C;C)
Significance	Other
Disease	46
Variation	info
Gene	NR5A1
CLNDBN	46,XY sex reversal, type 3 46,XX sex reversal 4
Reversed	1
HGVS	NC_000009.11:g.127262965G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000256210.1, RCV000490553.1,