DPY19L2, dpy-19 like 2, 283417

N. diseases: 4; N. variants: 5
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: rs147579680
rs147579680
1.000 12 63624124 missense variant C/T snv 1.7E-04 2.2E-04
CUI: C3151407
Disease: SPERMATOGENIC FAILURE 9
SPERMATOGENIC FAILURE 9
0.700 0
dbSNP: rs587777205
rs587777205
1.000 12 63569312 stop gained T/A;G snv 3.7E-05; 1.7E-04
CUI: C3151407
Disease: SPERMATOGENIC FAILURE 9
SPERMATOGENIC FAILURE 9
0.700 0
dbSNP: rs587777206
rs587777206
1.000 12 63624101 missense variant G/A snv 4.0E-06 7.0E-06
CUI: C3151407
Disease: SPERMATOGENIC FAILURE 9
SPERMATOGENIC FAILURE 9
0.700 0
dbSNP: rs751879424
rs751879424
1.000 12 63617339 frameshift variant A/- del 2.1E-05
CUI: C3151407
Disease: SPERMATOGENIC FAILURE 9
SPERMATOGENIC FAILURE 9
0.700 0
dbSNP: rs868256749
rs868256749
1.000 12 63617303 splice donor variant C/T snv
CUI: C3151407
Disease: SPERMATOGENIC FAILURE 9
SPERMATOGENIC FAILURE 9
0.700 0