Unknown
Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
GC∗1F NM_000583.4:c.[1296=;1307=] | 29 | 0.33 | ||
GC*1S NM_000583.4:c.[1296T>G;1307=] | 40 | 0.45 | ||
GC∗2 NM_000583.4:c.[1296=;1307C>A] | 9 | 0.1 | ||
GC∗3 NM_000583.4:c.[1296T>G;1307C>A] | 11 | 0.124 |
Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
---|---|---|---|---|---|---|
139200.G.1.2 | Lebanon | Unknown | Study participants with normal levels of vitamin D |