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: rs3805663
rs3805663
PITX1
2 1.000 0.120 5 135030510 intron variant A/G snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs4888262
rs4888262
RFWD3
2 1.000 0.120 16 74636560 synonymous variant C/T snv 0.54 0.59 0.700 1.000 1 2013 2013
dbSNP: rs7010162
rs7010162
PRDM14
2 1.000 0.120 8 70064270 intron variant C/T snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs8046148
rs8046148 		2 1.000 0.120 16 50109033 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs6671895
rs6671895
MIR3659 ; MIR3659HG
2 1.000 0.120 1 38089354 intron variant C/A;T snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs7532231
rs7532231 		2 1.000 0.120 1 104193445 intron variant A/G;T snv 0.39 0.700 1.000 1 2019 2019