Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_012407.4:c.283-176C>T | 47 | 0.208 | ||
NM_012407.4:c.283-59= | 75 | 0.329 | ||
NM_006457.5:c.1141A>G | 115 | 0.487 | ||
NM_006457.5:c.1162C>T | 1 | 0.004 | ||
NM_006457.5:c.*1006A>G | 118 | 0.527 | ||
NM_006457.5:c.*1054del | 86 | 0.37 | ||
NM_006457.5:c.*1061T>C | 79 | 0.341 | ||
NM_006457.5:c.407C>T | 52 | 0.215 | ||
NM_006457.5:c.1283+412G>A | 0.496 | |||
NM_001010848.4:c.1986C>T | 94 | 0.402 | ||
NM_001010848.4:c.1829T>G | 11 | 0.047 | ||
NM_018662.3:c.791G>A | 43 | 0.179 |
Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
---|---|---|---|---|---|---|
181500.G.2 | United Arab Emirates | Schizophrenia | 174 control subjects |