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: rs10206089
rs10206089 		4 2 61476184 intron variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1025687
rs1025687
MAPK4
3 18 50621423 intron variant T/C snv 0.61 0.700 1.000 1 2016 2016
dbSNP: rs10265538
rs10265538 		2 7 20502242 intergenic variant T/C snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs10283564
rs10283564
JAK2 ; INSL6
2 9 5075628 intron variant C/G snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs1032726
rs1032726
CD200R1
2 3 112967228 intron variant T/C snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs1036207
rs1036207
NDFIP1
3 1.000 0.080 5 142119476 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10409243
rs10409243
DNMT1 ; S1PR2
6 19 10222312 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10410864
rs10410864 		2 19 39711776 downstream gene variant T/C snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs10542411
rs10542411 		2 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 0.700 1.000 1 2016 2016
dbSNP: rs1059513
rs1059513
NAB2 ; STAT6
11 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs10667251
rs10667251 		4 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 0.700 1.000 1 2016 2016
dbSNP: rs10795656
rs10795656 		4 1.000 0.080 10 8553876 intergenic variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10852622
rs10852622
ZFPM1
2 16 88490472 intron variant A/G snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs10858740
rs10858740 		5 12 88451258 intergenic variant A/G;T snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs10905284
rs10905284
GATA3
4 0.882 0.200 10 8073399 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10995240
rs10995240
ZNF365 ; LOC105378327
2 10 62628871 intron variant G/C snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs10995477
rs10995477
JMJD1C
4 10 63250912 intron variant T/C snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs11127153
rs11127153
PLB1
2 2 28463094 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs111759324
rs111759324 		2 1 101186966 upstream gene variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs111930700
rs111930700
ACVR1B
4 12 51967869 intron variant C/G snv 8.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs11242709
rs11242709 		2 1.000 0.040 6 209159 upstream gene variant C/T snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs11253530
rs11253530
LOC107984285
1 10 947789 intergenic variant T/C snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs11317778
rs11317778
CHD1
1 5 98905525 intron variant AAA/-;AA;AAAA delins 0.27 0.700 1.000 1 2016 2016
dbSNP: rs11319879
rs11319879
HHEX
2 10 92693719 intron variant A/- delins 0.53 0.700 1.000 1 2016 2016
dbSNP: rs11327184
rs11327184
CCDC26
4 8 129592027 intron variant C/- delins 0.40 0.700 1.000 1 2016 2016