Unknown
Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_138691.2:c.100C>T | 2 |
Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
---|---|---|---|---|---|---|
600974.1.1 | Algeria | Hearing impairment | Unknown | |||
600974.1.2 | Algeria | Hearing impairment | Unknown | |||
600974.1.3 | Algeria | Hearing impairment | Unknown | |||
600974.1.4 | Algeria | Hearing impairment | Unknown | |||
600974.1.6 | Algeria | Hearing impairment | Unknown | |||
600974.1.7 | Algeria | Hearing impairment | Unknown | |||
600974.1.8 | Algeria | Hearing impairment | Unknown |