rs3762986
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3762986(C;C) |
| Make rs3762986(C;T) |
| Make rs3762986(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 96435158 |
| Gene | LOC101929710, PCSK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3762986 |
| dbSNP (classic) | rs3762986 |
| ClinGen | rs3762986 |
| ebi | rs3762986 |
| HLI | rs3762986 |
| Exac | rs3762986 |
| Gnomad | rs3762986 |
| Varsome | rs3762986 |
| LitVar | rs3762986 |
| Map | rs3762986 |
| PheGenI | rs3762986 |
| Biobank | rs3762986 |
| 1000 genomes | rs3762986 |
| hgdp | rs3762986 |
| ensembl | rs3762986 |
| geneview | rs3762986 |
| scholar | rs3762986 |
| rs3762986 | |
| pharmgkb | rs3762986 |
| gwascentral | rs3762986 |
| openSNP | rs3762986 |
| 23andMe | rs3762986 |
| SNPshot | rs3762986 |
| SNPdbe | rs3762986 |
| MSV3d | rs3762986 |
| GWAS Ctlg | rs3762986 |
| GMAF | 0.4977 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24618767] Epistasis between polymorphisms in PCSK1 and DBH is associated with premature ovarian failure
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d
