chr6:31967534:C>T Detail (hg38) (SKIC2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr6:31,935,311-31,935,311 View the variant detail on this assembly version. |
hg38 | chr6:31,967,534-31,967,534 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_006929.4:c.2583+157C>T | |
Ensemble | ENST00000375394.7:c.2583+157C>T | |
ENST00000491994.2:c.2583+157C>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.107 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.131 | age related macular degeneration | NA | GAD | Detail | |
0.125 | age related macular degeneration | The SKIV2L SNPs rs429608 and rs453821 were significantly associated with neovasc... | BeFree | 23260260 | Detail |
<0.001 | macular degeneration | The SKIV2L SNPs rs429608 and rs453821 were significantly associated with neovasc... | BeFree | 23260260 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NA | DisGeNET | Detail |
The SKIV2L SNPs rs429608 and rs453821 were significantly associated with neovascular AMD (P = 7.39 ×... | DisGeNET | Detail |
The SKIV2L SNPs rs429608 and rs453821 were significantly associated with neovascular AMD (P = 7.39 ×... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs453821 dbSNP
- Genome
- hg38
- Position
- chr6:31,967,534-31,967,534
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs453821
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.1069
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 1792
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
Genome browser