chr11:27694241:G>C Detail (hg19) (BDNF, BDNF-AS)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:27,694,241-27,694,241 |
hg38 | chr11:27,672,694-27,672,694 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001143810.1:c.225+1366C>G | |
NM_001143806.1:c.-21-14109C>G | ||
NM_001143805.1:c.-21-14109C>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
Likely risk allele | 2023-12-11 | no assertion criteria provided | post-traumatic stress disorder |
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Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_001709.5(BDNF):c.[*1785G>T;-21-14109C>G196G>A] AND Post-traumatic stress disorder | ClinVar | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs6265 dbSNP
- Genome
- hg19
- Position
- chr11:27,694,241-27,694,241
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- C
Genome browser