rs587777270
From SNPedia
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 |
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, |