rs730880018

Orientation

plus

Stabilized

plus

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

Make rs730880018(C;G)

Make rs730880018(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

91353299

Gene

HFM1

is a	snp
is	mentioned by
dbSNP	rs730880018
dbSNP (classic)	rs730880018
ClinGen	rs730880018
ebi	rs730880018
HLI	rs730880018
Exac	rs730880018
Gnomad	rs730880018
Varsome	rs730880018
LitVar	rs730880018
Map	rs730880018
PheGenI	rs730880018
Biobank	rs730880018
1000 genomes	rs730880018
hgdp	rs730880018
ensembl	rs730880018
geneview	rs730880018
scholar	rs730880018
google	rs730880018
pharmgkb	rs730880018
gwascentral	rs730880018
openSNP	rs730880018
23andMe	rs730880018
SNPshot	rs730880018
SNPdbe	rs730880018
MSV3d	rs730880018
GWAS Ctlg	rs730880018

Max Magnitude

0

ClinVar
Risk	rs730880018(G;G)
Alt	rs730880018(G;G)
Reference	Rs730880018(C;C)
Significance	Pathogenic
Disease	Premature ovarian failure 9
Variation	info
Gene	HFM1
CLNDBN	Premature ovarian failure 9
Reversed	0
HGVS	NC_000001.10:g.91818856C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000114368.2,