chr6:88872930:T>G Detail (hg19) (CNR1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr6:88,872,930-88,872,930 |
hg38 | chr6:88,163,211-88,163,211 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001160226.1:c.-64+2592A>C | |
NM_001160259.1:c.-64+2592A>C | ||
NM_016083.4:c.-64+2592A>C |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.285 | |
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 |
---|---|---|---|---|---|
0.007 | Marijuana Abuse | Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms ... | BeFree | 24407958 | Detail |
0.014 | Marijuana Abuse | Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms ... | BeFree | 24407958 | Detail |
<0.001 | Marijuana Abuse | Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms ... | BeFree | 24407958 | Detail |
0.002 | Marijuana Abuse | Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms ... | BeFree | 24407958 | Detail |
0.006 | Marijuana Abuse | Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms ... | BeFree | 24407958 | Detail |
0.003 | Marijuana Abuse | Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms ... | BeFree | 24407958 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms (SNP) of the CNR1 (r... | DisGeNET | Detail |
Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms (SNP) of the CNR1 (r... | DisGeNET | Detail |
Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms (SNP) of the CNR1 (r... | DisGeNET | Detail |
Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms (SNP) of the CNR1 (r... | DisGeNET | Detail |
Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms (SNP) of the CNR1 (r... | DisGeNET | Detail |
Here, we made a preliminary screening among ten Single Nucleotide Polymorphisms (SNP) of the CNR1 (r... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs6454674 dbSNP
- Genome
- hg19
- Position
- chr6:88,872,930-88,872,930
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- G
- 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))
- rs6454674
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.2851
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 4778
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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