Genomic variant #0000826645
Individual ID |
00000003 |
Chromosome |
X |
Allele |
Unknown |
Affects function (reported) |
Not classified |
Affects function (concluded) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.75114852T>C |
Reference |
dbSNP |
DB-ID |
ABCB7_000021 |
Frequency |
0.137 |
Allele Count |
29 |
Allele Number |
212 |
Depth |
3213 |
Average frequency (large NGS studies) |
Variant not found in online data sets |
Owner |
Admin |
Variant on transcripts
Screenings
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