LIN28B, lin-28 homolog B, 389421

N. diseases: 126; N. variants: 24
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs314263
rs314263
6 104944870 intron variant C/T snv 0.69
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018