rs606231206

Orientation

minus

Stabilized

minus

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

Make rs606231206(-;-)

Make rs606231206(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

124500294

Gene

NR5A1

is a	snp
is	mentioned by
dbSNP	rs606231206
dbSNP (classic)	rs606231206
ClinGen	rs606231206
ebi	rs606231206
HLI	rs606231206
Exac	rs606231206
Gnomad	rs606231206
Varsome	rs606231206
LitVar	rs606231206
Map	rs606231206
PheGenI	rs606231206
Biobank	rs606231206
1000 genomes	rs606231206
hgdp	rs606231206
ensembl	rs606231206
geneview	rs606231206
scholar	rs606231206
google	rs606231206
pharmgkb	rs606231206
gwascentral	rs606231206
openSNP	rs606231206
23andMe	rs606231206
SNPshot	rs606231206
SNPdbe	rs606231206
MSV3d	rs606231206
GWAS Ctlg	rs606231206

Max Magnitude

0

ClinVar
Risk	rs606231206(-;-)
Alt	rs606231206(-;-)
Reference	Rs606231206(C;C)
Significance	Pathogenic
Disease	46 Premature ovarian failure 7
Variation	info
Gene	NR5A1
CLNDBN	46,XY sex reversal, type 3 Premature ovarian failure 7
Reversed	1
HGVS	NC_000009.11:g.127262573delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013648.24, RCV000013649.19,