Variant #0000695812 (NC_000012.11:g.40637333A>G, NC_000012.11(NM_198578.3):c.707-19A>G (LRRK2))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.40637333A>G |
| DNA change (hg38) |
g.40243531A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
LRRK2_000092 |
| Variant remarks |
- |
| Reference |
PubMed: Rubio 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
1/27874 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Justin Rubio |
| Database submission license |
No license selected |
| Created by |
Justin Rubio |
| Date created |
2012-04-27 21:16:32 +02:00 (CEST) |
| Date last edited |
2020-10-03 11:32:58 +02:00 (CEST) |

Variant on transcripts
Screenings
|