rs4837864
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4837864(C;C) |
Make rs4837864(C;T) |
Make rs4837864(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 116782154 |
Gene | ASTN2 |
is a | snp |
is | mentioned by |
dbSNP | rs4837864 |
dbSNP (classic) | rs4837864 |
ClinGen | rs4837864 |
ebi | rs4837864 |
HLI | rs4837864 |
Exac | rs4837864 |
Gnomad | rs4837864 |
Varsome | rs4837864 |
LitVar | rs4837864 |
Map | rs4837864 |
PheGenI | rs4837864 |
Biobank | rs4837864 |
1000 genomes | rs4837864 |
hgdp | rs4837864 |
ensembl | rs4837864 |
geneview | rs4837864 |
scholar | rs4837864 |
rs4837864 | |
pharmgkb | rs4837864 |
gwascentral | rs4837864 |
openSNP | rs4837864 |
23andMe | rs4837864 |
SNPshot | rs4837864 |
SNPdbe | rs4837864 |
MSV3d | rs4837864 |
GWAS Ctlg | rs4837864 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25083881] Endometriosis Is Associated with Rare Copy Number Variants
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 9
- 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