chr8:42271987:A>G Detail (hg38) (IKBKB)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr8:42,129,505-42,129,505 View the variant detail on this assembly version. |
hg38 | chr8:42,271,987-42,271,987 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001556.2:c.-18-96A>G | |
NR_040009.1:c.-18-96A>G | ||
NM_001190720.2:c.-88+518A>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | Wheezing | IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were asso... | BeFree | 25326706 | Detail |
<0.001 | Wheezing | IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were asso... | BeFree | 25326706 | Detail |
<0.001 | Wheezing | IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were asso... | BeFree | 25326706 | Detail |
0.001 | Wheezing | IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were asso... | BeFree | 25326706 | Detail |
<0.001 | Wheezing | IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were asso... | BeFree | 25326706 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were associated with a signif... | DisGeNET | Detail |
IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were associated with a signif... | DisGeNET | Detail |
IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were associated with a signif... | DisGeNET | Detail |
IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were associated with a signif... | DisGeNET | Detail |
IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were associated with a signif... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs3747811 dbSNP
- Genome
- hg38
- Position
- chr8:42,271,987-42,271,987
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
Genome browser