Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137854889
rs137854889
ZMPSTE24
31 0.742 0.440 1 40290871 frameshift variant T/-;TT delins 0.700 0
dbSNP: rs886039909
rs886039909
HSPG2
6 0.882 0.120 1 21864095 splice region variant C/T snv 0.700 0
dbSNP: rs797044484
rs797044484
TP63
10 0.776 0.400 3 189868624 missense variant C/G snv 0.700 1.000 1 2010 2010
dbSNP: rs879253745
rs879253745
ARID1B
6 0.925 0.240 6 157181040 frameshift variant AA/- delins 0.700 0
dbSNP: rs879253746
rs879253746
ARID1B
6 0.925 0.240 6 157200866 frameshift variant -/T delins 0.700 0
dbSNP: rs879253747
rs879253747
ARID1B
6 0.925 0.240 6 157167101 stop gained C/T snv 0.700 0
dbSNP: rs879253856
rs879253856
ARID1B
6 0.925 0.240 6 157110496 frameshift variant CCG/TCCGCAGCCACTCC delins 0.700 0
dbSNP: rs1057516033
rs1057516033
KAT6B
9 0.807 0.400 10 75025250 splice donor variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1554844486
rs1554844486
KAT6B
10 0.827 0.160 10 75024984 frameshift variant GGGT/- del 0.700 0
dbSNP: rs1555154946
rs1555154946
ARID2 ; LOC105369745
16 0.827 0.120 12 45850644 stop gained C/T snv 0.700 0
dbSNP: rs1223073957
rs1223073957
MED25
12 0.827 0.240 19 49835897 frameshift variant C/- delins 1.2E-05 1.4E-05 0.700 0
dbSNP: rs776291104
rs776291104
MED25
12 0.827 0.240 19 49829816 missense variant C/T snv 8.7E-06 0.700 0
dbSNP: rs1556914274
rs1556914274
HUWE1
13 0.790 0.440 X 53537626 missense variant G/A snv 0.700 0
dbSNP: rs1557006903
rs1557006903
HUWE1
5 0.851 0.280 X 53615815 missense variant C/T snv 0.700 0
dbSNP: rs1569509136
rs1569509136
HUWE1
24 0.708 0.400 X 53647576 splice acceptor variant T/C snv 0.700 0