Exomes | Genomes | Total | |
---|---|---|---|
Filters | Pass | Pass | |
Allele Count | 604 | 45 | 649 |
Allele Number | 1461824 | 152330 | 1614154 |
Allele Frequency | 0.0004132 | 0.0002954 | 0.0004021 |
Grpmax Filtering AF (95% confidence) | 0.0004685 European (non-Finnish) | 0.0003540 European (non-Finnish) | 0.0004686 European (non-Finnish) |
Number of homozygotes | 2 | 0 | 2 |
593 | 1180020 | 2 | 0.0005025 | ||
23 | 60026 | 0 | 0.0003832 | ||
20 | 62512 | 0 | 0.0003199 | ||
7 | 75050 | 0 | 0.00009327 | ||
5 | 63996 | 0 | 0.00007813 | ||
1 | 29608 | 0 | 0.00003377 | ||
0 | 44882 | 0 | 0.000 | ||
0 | 6062 | 0 | 0.000 | ||
0 | 912 | 0 | 0.000 | ||
0 | 91086 | 0 | 0.000 | ||
XX | 326 | 812442 | 1 | 0.0004013 | |
XY | 323 | 801712 | 1 | 0.0004029 | |
Total | 649 | 1614154 | 2 | 0.0004021 |
The following GRCh37 variant lifts over to this variant:
This variant falls on 20 transcripts in 1 gene.
Note The gene symbols shown below are provided by VEP and may differ from the symbol shown on gene pages.
or find more information on the ClinVar website. Data displayed here is from ClinVar's February 1, 2025 release.
Value: 7.004e+5 (exome samples), 4.427e+4 (genome samples)
Site quality approximation for all variants with 0.0002 <= AF < 0.0005.
Note: These are site-level quality metrics, they may be unpredictable for multi-allelic sites.