Variant #0001029811 (NC_000006.11:g.40997833G>T)
| Individual ID |
00464366 |
| Chromosome |
6 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
association |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.40997833G>T |
| DNA change (hg38) |
g.41030094G>T |
| Published as |
- |
| ISCN |
6p21.1-p12.3 |
| DB-ID |
chr6_008173 |
| Variant remarks |
LOD score 1.92 |
| Reference |
PMID:Yousaf 2024:39334596 |
| ClinVar ID |
- |
| dbSNP ID |
rs736794 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Sahib Kaloti |
| Database submission license |
No license selected |
| Created by |
Sahib Kaloti |
| Date created |
2025-03-07 23:21:07 +01:00 (CET) |
| Date last edited |
2025-03-12 11:36:04 +01:00 (CET) |

Variant on transcripts
Screenings
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