Variant #0000876302 (NC_000005.9:g.178421770T>G, NM_000843.3:c.176A>C (GRM6))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.178421770T>G |
| DNA change (hg38) |
- |
| Published as |
c.176A>C |
| ISCN |
- |
| DB-ID |
GRM6_000033 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Xu 2009 |
| ClinVar ID |
- |
| dbSNP ID |
rs2645329 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
76/96 patients with high myopia |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.54981 View details |
| Owner |
LOVD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2022-08-15 15:41:08 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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