rs587777270

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(CC;CC)	0	common in clinvar
(CCC;CCC)	0	common in clinvar
(GG;GG)	0	common in clinvar

Make rs587777270(C;C)

Make rs587777270(C;GG)

Reference

GRCh38 38.1/142

Chromosome

1

Position

91266061

Gene

HFM1

is a	snp
is	mentioned by
dbSNP	rs587777270
dbSNP (classic)	rs587777270
ClinGen	rs587777270
ebi	rs587777270
HLI	rs587777270
Exac	rs587777270
Gnomad	rs587777270
Varsome	rs587777270
LitVar	rs587777270
Map	rs587777270
PheGenI	rs587777270
Biobank	rs587777270
1000 genomes	rs587777270
hgdp	rs587777270
ensembl	rs587777270
geneview	rs587777270
scholar	rs587777270
google	rs587777270
pharmgkb	rs587777270
gwascentral	rs587777270
openSNP	rs587777270
23andMe	rs587777270
SNPshot	rs587777270
SNPdbe	rs587777270
MSV3d	rs587777270
GWAS Ctlg	rs587777270

Max Magnitude

0

ClinVar
Risk	rs587777270(C;C) Rs587777270(GG;GG)
Alt	rs587777270(C;C) Rs587777270(GG;GG)
Reference	Rs587777270(CC;CC)
Significance	Pathogenic
Disease	Premature ovarian failure 9
Variation	info
Gene	HFM1
CLNDBN	Premature ovarian failure 9
Reversed	1
HGVS	NC_000001.10:g.91731618_91731619delGGinsC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000114371.3,