Human SNP ID | rs56219066 |
---|---|
Human chromosome | chr5 |
Human SNP position | 95907227 |
Pig chromosome | chr2 |
Pig SNP position | 106424421 |
PubMed ID | 26007630 |
---|---|
Journal | Nat Commun |
Link | www.ncbi.nlm.nih.gov/pubmed/26007630 |
Study | Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. |
Disease/Trait | Multiple myeloma |
Initial sample | 2,194 European ancestry cases, 222,555 European ancestry controls |
Replication sample | 586 European ancestry cases, 2,111 European ancestry controls |
Region | 5q15 |
Chromosome id | chr5 |
Chromosome position | 95907227 |
Reported gene | ELL2 |
Mapped gene | ELL2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 22936 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs56219066-T |
SNPs | rs56219066 |
Merged | |
SNP id current | 56219066 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.711 |
P value | 0.000000001 |
Pvalue mlog | 9 |
P value text | |
Or beta | 1.25 |
%95 Ci | [1.16-1.34] |
Platform | Illumina [12100000] (imputed) |
CNV | N |
Mapped trait | multiple myeloma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001378 |
Study accession | GCST002921 |
PubMed ID | 26007630 |
Journal | Nat Commun |
Link | www.ncbi.nlm.nih.gov/pubmed/26007630 |
Study | Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. |
Disease/Trait | Multiple myeloma and monoclonal gammopathy |
Initial sample | 2,194 European ancestry multiple myeloma cases, 251 European ancestry monoclonal gammopathy cases, 294,390 European ancestry controls |
Replication sample | 586 European ancestry multiple myeloma cases, 2,111 European ancestry controls |
Region | 5q15 |
Chromosome id | chr5 |
Chromosome position | 95907227 |
Reported gene | ELL2 |
Mapped gene | ELL2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 22936 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs56219066-T |
SNPs | rs56219066 |
Merged | |
SNP id current | 56219066 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.711 |
P value | 0.0000000002 |
Pvalue mlog | 9.69897000433601 |
P value text | |
Or beta | 1.24 |
%95 Ci | [1.16-1.33] |
Platform | Illumina [12100000] (imputed) |
CNV | N |
Mapped trait | multiple myeloma, monoclonal gammopathy |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001378, http://www.ebi.ac.uk/efo/EFO_0000203 |
Study accession | GCST002922 |