rs587777268

Orientation

plus

Stabilized

plus

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

Make rs587777268(A;C)

Make rs587777268(C;C)

Reference

GRCh38 38.1/142

Chromosome

1

Position

91319322

Gene

HFM1

is a	snp
is	mentioned by
dbSNP	rs587777268
dbSNP (classic)	rs587777268
ClinGen	rs587777268
ebi	rs587777268
HLI	rs587777268
Exac	rs587777268
Gnomad	rs587777268
Varsome	rs587777268
LitVar	rs587777268
Map	rs587777268
PheGenI	rs587777268
Biobank	rs587777268
1000 genomes	rs587777268
hgdp	rs587777268
ensembl	rs587777268
geneview	rs587777268
scholar	rs587777268
google	rs587777268
pharmgkb	rs587777268
gwascentral	rs587777268
openSNP	rs587777268
23andMe	rs587777268
SNPshot	rs587777268
SNPdbe	rs587777268
MSV3d	rs587777268
GWAS Ctlg	rs587777268

Max Magnitude

0

ClinVar
Risk	rs587777268(C;C)
Alt	rs587777268(C;C)
Reference	Rs587777268(A;A)
Significance	Pathogenic
Disease	Premature ovarian failure 9
Variation	info
Gene	HFM1
CLNDBN	Premature ovarian failure 9
Reversed	0
HGVS	NC_000001.10:g.91784879A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000114369.3,