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: rs267607016
rs267607016
ROR2
3 0.882 0.120 9 91726603 stop gained G/A snv 4.0E-06 1.4E-05 0.010 1.000 1 2009 2009
dbSNP: rs1555528356
rs1555528356
ANKRD11
13 0.790 0.360 16 89282836 stop gained G/A snv 0.700 0
dbSNP: rs387906836
rs387906836
TULP1
5 0.851 0.080 6 35503763 missense variant G/A snv 0.700 0
dbSNP: rs764926983
rs764926983
DYNC2H1
9 0.882 0.120 11 103287559 synonymous variant G/A snv 1.2E-05 0.700 0
dbSNP: rs863225094
rs863225094
PPP2R1A
10 0.827 0.160 19 52213076 missense variant G/A snv 0.700 0
dbSNP: rs140047318
rs140047318
BMPR1B
3 0.882 0.080 4 95152757 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs886040971
rs886040971
TRPS1
56 0.683 0.280 8 115604339 stop gained G/A;T snv 0.700 0
dbSNP: rs1014959895
rs1014959895
PRMT7
16 0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs397507520
rs397507520
PTPN11
39 0.658 0.520 12 112453279 missense variant G/C;T snv 0.700 0
dbSNP: rs587784000
rs587784000
NIPBL
5 0.882 0.120 5 37044480 missense variant G/C;T snv 0.700 0
dbSNP: rs1554888939
rs1554888939
EHMT1
58 0.683 0.640 9 137798823 missense variant G/T snv 0.700 0
dbSNP: rs371011047
rs371011047
DYNC2H1
9 0.882 0.120 11 103120982 stop gained G/T snv 2.8E-05 0.700 0
dbSNP: rs1556165162
rs1556165162
HDAC8
7 0.882 0.120 X 72572657 frameshift variant GG/- delins 0.700 0
dbSNP: rs1565311145
rs1565311145
DYNC2H1
7 0.882 0.120 11 103116677 stop gained T/A snv 0.700 0
dbSNP: rs1553154130
rs1553154130
RERE
18 0.807 0.280 1 8358231 missense variant T/A;C snv 0.700 0
dbSNP: rs61752717
rs61752717
MEFV
72 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 0.700 0
dbSNP: rs398123425
rs398123425
ATRX
9 0.776 0.320 X 77688876 missense variant T/C snv 0.700 0
dbSNP: rs775769424
rs775769424
BBS1 ; ZDHHC24
11 0.776 0.280 11 66530934 frameshift variant TG/- del 1.4E-05 0.700 0