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: rs10076436
rs10076436 		1 5 154492281 upstream gene variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10799792
rs10799792
LUZP1
1 1 23119948 intron variant T/G snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs11039216
rs11039216
SPI1
3 11 47385041 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1124477
rs1124477 		1 12 114911692 intergenic variant T/C snv 0.71 0.700 1.000 1 2018 2018
dbSNP: rs13165478
rs13165478 		3 5 154489480 upstream gene variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs1415259
rs1415259
NOS1AP ; LOC105371475
5 0.925 0.080 1 162115519 intron variant C/T snv 0.54 0.700 1.000 1 2010 2010
dbSNP: rs2042400
rs2042400
LINC02137
1 16 58430436 intron variant T/C snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs2098226
rs2098226
ACTB
1 7 5543414 intron variant A/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs2207793
rs2207793
NFIA
1 1 61428981 intron variant C/T snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs4966020
rs4966020
IGF1R
3 0.925 0.120 15 98741451 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs6795970
rs6795970
SCN10A
13 0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 0.700 1.000 1 2010 2010
dbSNP: rs7029396
rs7029396
HMCN2
1 9 130263971 upstream gene variant C/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs7301677
rs7301677 		1 12 114943342 intergenic variant C/T snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs7638275
rs7638275
SCN5A
1 3 38624332 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7966951
rs7966951 		1 12 114927406 downstream gene variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs882300
rs882300
LOC107985947
3 1.000 0.080 2 136218685 intergenic variant T/C;G snv 0.700 1.000 1 2007 2007