Disease: Feeding difficulties in infancy
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1085307845
PHIP
0.752 0.320 6 79025582 missense variant G/T snv 21
rs1562114190
IRAK1BP1 ; PHIP
0.790 0.160 6 78946061 frameshift variant A/- delins 21
rs1057524157
DEAF1
0.776 0.200 11 686962 missense variant A/C;T snv 19
rs142110773
FIGNL1 ; DDC
0.882 0.160 7 50463317 missense variant G/A snv 1.6E-05 7.0E-06 13
rs1562171209
PHIP
0.851 0.160 6 79003821 missense variant T/C snv 9