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: rs10195252
rs10195252
COBLL1
7 0.925 0.080 2 164656581 intron variant T/C snv 0.48 0.800 1.000 5 2010 2019
dbSNP: rs11724804
rs11724804
DGKQ
4 0.882 0.160 4 971991 intron variant G/A snv 0.43 0.700 1.000 3 2018 2019
dbSNP: rs1190982
rs1190982
ARID4A
1 14 58349121 intron variant T/C snv 0.68 0.700 1.000 3 2018 2019
dbSNP: rs1294410
rs1294410
LOC101928004
3 6 6738519 intron variant T/C snv 0.65 0.800 1.000 3 2013 2019
dbSNP: rs13028903
rs13028903 		1 2 59724330 intron variant C/T snv 0.41 0.700 1.000 3 2018 2019
dbSNP: rs1569135
rs1569135
LOC105373786
3 2 187250671 intron variant A/G snv 0.51 0.700 1.000 3 2015 2019
dbSNP: rs17326656
rs17326656
LHCGR ; STON1-GTF2A1L
1 2 48735152 intron variant G/T snv 0.21 0.700 1.000 3 2018 2019
dbSNP: rs2167750
rs2167750
FAM13A
1 4 88808923 intron variant C/T snv 0.50 0.700 1.000 3 2018 2019
dbSNP: rs2294239
rs2294239
ZNRF3
4 22 29053489 intron variant A/G snv 0.36 0.700 1.000 3 2018 2019
dbSNP: rs2925979
rs2925979
CMIP
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs3786897
rs3786897
PEPD
5 1.000 0.080 19 33402102 intron variant A/G snv 0.45 0.700 1.000 3 2015 2019
dbSNP: rs905938
rs905938
ZBTB7B ; DCST2
5 1 155018913 intron variant T/C snv 0.24 0.700 1.000 3 2018 2019
dbSNP: rs1011731
rs1011731
PIGC ; DNM3
4 1 172377408 intron variant G/A snv 0.46 0.800 1.000 2 2010 2015
dbSNP: rs10745659
rs10745659
CRADD
1 12 93698914 intron variant C/A;G snv 0.700 1.000 2 2018 2019
dbSNP: rs10795055
rs10795055
LOC105376360
1 10 3539029 intron variant A/G snv 0.54 0.700 1.000 2 2019 2019
dbSNP: rs10980797
rs10980797
LOC105376219
3 9 111150273 intron variant A/G;T snv 0.700 1.000 2 2019 2019
dbSNP: rs1105881
rs1105881
MAPKBP1
1 15 41780332 intron variant C/G snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs11079041
rs11079041
STAT5B
4 0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 0.700 1.000 2 2018 2019
dbSNP: rs11187537
rs11187537
FFAR4
1 10 93587048 intron variant G/C snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs11747001
rs11747001
HSPA4
1 5 133076607 intron variant A/G snv 0.21 0.21 0.700 1.000 2 2018 2019
dbSNP: rs11992444
rs11992444 		1 8 25607174 intron variant G/T snv 0.49 0.700 1.000 2 2019 2019
dbSNP: rs12459350
rs12459350
DOT1L
3 0.925 0.200 19 2176587 intron variant A/G snv 0.46 0.700 1.000 2 2018 2019
dbSNP: rs12631066
rs12631066
PDCD6IP
1 3 33831295 intron variant G/C;T snv 0.700 1.000 2 2018 2019
dbSNP: rs12684047
rs12684047
EPB41L4B
1 9 109210391 intron variant T/A snv 0.15 0.700 1.000 2 2018 2019
dbSNP: rs13256367
rs13256367
POU5F1B ; CASC8 ; PCAT1 ; CASC21
1 8 127322655 intron variant A/C;T snv 0.700 1.000 2 2018 2019