Sequence Name | Change(s) |
---|---|
GRCh38.p7 chr 9 | NC_000009.12:g.7026716G>A |
GRCh37.p13 chr 9 | NC_000009.11:g.7026716G>A |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
KDM4C transcript variant 3 | NM_001146695.1:c. | N/A | Intron Variant |
KDM4C transcript variant 4 | NM_001146696.1:c. | N/A | Intron Variant |
KDM4C transcript variant 5 | NM_001304339.1:c. | N/A | Intron Variant |
KDM4C transcript variant 6 | NM_001304340.1:c. | N/A | Intron Variant |
KDM4C transcript variant 1 | NM_015061.3:c. | N/A | Intron Variant |
KDM4C transcript variant 7 | NM_001304341.1:c. | N/A | Genic Downstream Transcript Variant |
KDM4C transcript variant 8 | NR_130707.1:n. | N/A | Genic Downstream Transcript Variant |
KDM4C transcript variant X1 | XM_006716741.2:c. | N/A | Intron Variant |
KDM4C transcript variant X4 | XM_011517811.2:c. | N/A | Intron Variant |
KDM4C transcript variant X6 | XM_011517812.2:c. | N/A | Intron Variant |
KDM4C transcript variant X14 | XM_011517816.2:c. | N/A | Intron Variant |
KDM4C transcript variant X2 | XM_017014498.1:c. | N/A | Intron Variant |
KDM4C transcript variant X3 | XM_017014499.1:c. | N/A | Intron Variant |
KDM4C transcript variant X5 | XM_017014500.1:c. | N/A | Intron Variant |
KDM4C transcript variant X7 | XM_017014501.1:c. | N/A | Intron Variant |
KDM4C transcript variant X9 | XM_017014502.1:c. | N/A | Intron Variant |
KDM4C transcript variant X13 | XM_017014503.1:c. | N/A | Intron Variant |
KDM4C transcript variant X15 | XM_017014504.1:c. | N/A | Intron Variant |
KDM4C transcript variant X16 | XM_017014505.1:c. | N/A | Intron Variant |
KDM4C transcript variant X17 | XM_017014506.1:c. | N/A | Intron Variant |
KDM4C transcript variant X8 | XR_001746252.1:n. | N/A | Intron Variant |
KDM4C transcript variant X10 | XR_001746253.1:n. | N/A | Intron Variant |
KDM4C transcript variant X11 | XR_001746254.1:n. | N/A | Intron Variant |
KDM4C transcript variant X12 | XR_001746255.1:n. | N/A | Intron Variant |
Study | Population | Group | Sample # | Ref Allele | Alt Allele |
---|---|---|---|---|---|
1000Genomes | African | Sub | 1322 | G=0.413 | A=0.587 |
1000Genomes | American | Sub | 694 | G=0.460 | A=0.540 |
1000Genomes | East Asian | Sub | 1008 | G=0.433 | A=0.567 |
1000Genomes | Europe | Sub | 1006 | G=0.551 | A=0.449 |
1000Genomes | Global | Study-wide | 5008 | G=0.424 | A=0.576 |
1000Genomes | South Asian | Sub | 978 | G=0.280 | A=0.720 |
The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 3854 | G=0.511 | A=0.489 |
The Genome Aggregation Database | African | Sub | 8682 | G=0.412 | A=0.588 |
The Genome Aggregation Database | American | Sub | 834 | G=0.470 | A=0.530 |
The Genome Aggregation Database | East Asian | Sub | 1600 | G=0.464 | A=0.536 |
The Genome Aggregation Database | Europe | Sub | 18432 | G=0.499 | A=0.500 |
The Genome Aggregation Database | Global | Study-wide | 29850 | G=0.472 | A=0.527 |
The Genome Aggregation Database | Other | Sub | 302 | G=0.620 | A=0.380 |
Trans-Omics for Precision Medicine | Global | Study-wide | 29118 | G=0.473 | A=0.526 |
UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | G=0.501 | A=0.499 |
SNP ID | p-value | Traits | Study |
---|---|---|---|
rs10975990 | 7.15E-06 | alcohol withdrawal symptoms | 22072270 |
Position (v37) | eGene | GeneID | Variant | p-value | TSS | Tissue | |
---|---|---|---|---|---|---|---|
There is no eQTL annotation for this SNP |
Probe ID | Position | Gene | beta | p-value | |||
---|---|---|---|---|---|---|---|
There is no meQTL annotation for this SNP |
There is no significant Hi-C chromatin interaction data for this SNP.
Chromosome | Start | End | Region | Distance ( -/+ : Up/Downstream ) |
---|---|---|---|---|
chr9 | 6978641 | 6978691 | E067 | -48025 |
chr9 | 6978754 | 6978915 | E067 | -47801 |
chr9 | 7052503 | 7053138 | E068 | 25787 |
chr9 | 7056766 | 7057012 | E068 | 30050 |
chr9 | 7057223 | 7057335 | E068 | 30507 |
chr9 | 7057342 | 7057422 | E068 | 30626 |
chr9 | 7057457 | 7058000 | E068 | 30741 |
chr9 | 7058090 | 7058230 | E068 | 31374 |
chr9 | 7058310 | 7058379 | E068 | 31594 |
chr9 | 7058388 | 7058453 | E068 | 31672 |
chr9 | 7058500 | 7058568 | E068 | 31784 |
chr9 | 7052503 | 7053138 | E069 | 25787 |
chr9 | 7053246 | 7053364 | E069 | 26530 |
chr9 | 7053377 | 7053446 | E069 | 26661 |
chr9 | 7053484 | 7053547 | E069 | 26768 |
chr9 | 7057457 | 7058000 | E069 | 30741 |
chr9 | 7058090 | 7058230 | E069 | 31374 |
chr9 | 7037273 | 7037323 | E070 | 10557 |
chr9 | 6978641 | 6978691 | E071 | -48025 |
chr9 | 6978754 | 6978915 | E071 | -47801 |
chr9 | 7052503 | 7053138 | E073 | 25787 |
chr9 | 7053246 | 7053364 | E073 | 26530 |
chr9 | 7053377 | 7053446 | E073 | 26661 |
chr9 | 6999991 | 7000124 | E074 | -26592 |
chr9 | 7056387 | 7056589 | E074 | 29671 |
chr9 | 7056766 | 7057012 | E074 | 30050 |
chr9 | 7057457 | 7058000 | E074 | 30741 |
chr9 | 7052503 | 7053138 | E081 | 25787 |
chr9 | 7053246 | 7053364 | E081 | 26530 |
chr9 | 7053377 | 7053446 | E081 | 26661 |
chr9 | 7053246 | 7053364 | E082 | 26530 |
chr9 | 7053377 | 7053446 | E082 | 26661 |
chr9 | 7055053 | 7055161 | E082 | 28337 |