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: rs314277
rs314277
0.925 0.080 6 104959787 intron variant A/C;G;T snv
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.700 1.000 1 2009 2009
dbSNP: rs395962
rs395962
6 104949543 intron variant T/G snv 0.72
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.700 1.000 1 2018 2018