rs77587352

Orientation

plus

Stabilized

plus

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

Make rs77587352(A;A)

Make rs77587352(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

144401890

Gene

NOBOX

is a	snp
is	mentioned by
dbSNP	rs77587352
dbSNP (classic)	rs77587352
ClinGen	rs77587352
ebi	rs77587352
HLI	rs77587352
Exac	rs77587352
Gnomad	rs77587352
Varsome	rs77587352
LitVar	rs77587352
Map	rs77587352
PheGenI	rs77587352
Biobank	rs77587352
1000 genomes	rs77587352
hgdp	rs77587352
ensembl	rs77587352
geneview	rs77587352
scholar	rs77587352
google	rs77587352
pharmgkb	rs77587352
gwascentral	rs77587352
openSNP	rs77587352
23andMe	rs77587352
SNPshot	rs77587352
SNPdbe	rs77587352
MSV3d	rs77587352
GWAS Ctlg	rs77587352

Max Magnitude

0

ClinVar
Risk	rs77587352(A;A)
Alt	rs77587352(A;A)
Reference	Rs77587352(C;C)
Significance	Pathogenic
Disease	Premature ovarian failure 5
Variation	info
Gene	NOBOX
CLNDBN	Premature ovarian failure 5
Reversed	0
HGVS	NC_000007.13:g.144098983C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000154190.4,