Variant #0000127690 (NC_000001.10:g.94586533T>G, NC_000001.10(NM_000350.2):c.66+3A>C (ABCA4))
| Chromosome |
1 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94586533T>G |
| DNA change (hg38) |
g.94120977T>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ABCA4_000254 See all 2 reported entries |
| Variant remarks |
variant significantly enriched in >3000 likely Caucasian STGD1 patients compared to the non-Finnish ExAC population |
| Reference |
PubMed: Cornelis 2017, Journal: Cornelis 2017, Journal: Cornelis 2023 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Stéphanie Cornelis |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Stéphanie Cornelis |
| Date created |
2016-07-29 12:46:24 +02:00 (CEST) |
| Date last edited |
2024-09-25 14:18:42 +02:00 (CEST) |

Variant on transcripts
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