Male
Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_005957.4:c.665C>T | 1 | |||
NM_000130.4:c.1601G>A | 1 | |||
NM_000506.4:c.*97G>A | 1 | |||
NM_000789.4:c.2306-105_2306-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | 1 | |||
NM_000602.5:c.-820G[(4_5)] | 1 |