chr8:35741644:A>G Detail (hg19)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr8:35,741,644-35,741,644 |
hg38 | chr8:35,884,126-35,884,126 View the variant detail on this assembly version. |
HGVS
[No Data.]
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.022 | Malignant neoplasm of breast | Seven single nucleotide polymorphisms (SNPs) (rs3856806 in PPARG, rs7014346 in P... | BeFree | 24338422 | Detail |
0.008 | breast carcinoma | Seven single nucleotide polymorphisms (SNPs) (rs3856806 in PPARG, rs7014346 in P... | BeFree | 24338422 | Detail |
0.127 | Malignant neoplasm of breast | Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN... | BeFree | 24338422 | Detail |
0.001 | breast carcinoma | Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN... | BeFree | 24338422 | Detail |
0.004 | breast carcinoma | Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN... | BeFree | 24338422 | Detail |
0.001 | Malignant neoplasm of breast | Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN... | BeFree | 24338422 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Seven single nucleotide polymorphisms (SNPs) (rs3856806 in PPARG, rs7014346 in POU5F1P1, rs989902 in... | DisGeNET | Detail |
Seven single nucleotide polymorphisms (SNPs) (rs3856806 in PPARG, rs7014346 in POU5F1P1, rs989902 in... | DisGeNET | Detail |
Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN13, and rs7003146 in... | DisGeNET | Detail |
Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN13, and rs7003146 in... | DisGeNET | Detail |
Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN13, and rs7003146 in... | DisGeNET | Detail |
Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN13, and rs7003146 in... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs7003146 dbSNP
- Genome
- hg19
- Position
- chr8:35,741,644-35,741,644
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
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