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: rs10950393
rs10950393
TMEM106B
2 1.000 0.040 7 12223920 intron variant T/C snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs11039409
rs11039409
NUP160
2 1.000 0.040 11 47814169 intron variant A/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs11123857
rs11123857
NPAS2
2 2 100987350 non coding transcript exon variant A/G snv 0.29 0.010 1.000 1 2010 2010
dbSNP: rs11152363
rs11152363
TCF4
2 1.000 0.040 18 55389957 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11209175
rs11209175
GNG12-AS1
2 1.000 0.040 1 67909145 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs11214589
rs11214589
TTC12
2 1.000 0.040 11 113374326 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs11214607
rs11214607
DRD2
2 1.000 0.040 11 113441417 intron variant T/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11514731
rs11514731
MAD1L1
2 1.000 0.040 7 2011868 intron variant C/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11599236
rs11599236
SORCS3
2 1.000 0.040 10 104694914 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs11605020
rs11605020
LOC105369562
2 1.000 0.040 11 127110970 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11608355
rs11608355
MYO1H
2 1.000 0.040 12 109441487 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs116362708
rs116362708
SLC44A5
2 1.000 0.040 1 75464629 intron variant G/A snv 2.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs11663393
rs11663393
DCC
2 1.000 0.040 18 53088362 intron variant G/A snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs11664123
rs11664123
DCC
2 1.000 0.040 18 53440658 intron variant T/C snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs11693031
rs11693031
ERBB4
2 1.000 0.040 2 211813206 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11826064
rs11826064 		2 1.000 0.040 11 50818695 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12030991
rs12030991 		2 1.000 0.040 1 106683737 intergenic variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12068879
rs12068879
KAZN
2 1.000 0.040 1 14959860 intron variant A/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs12137398
rs12137398
CAMTA1
2 1.000 0.040 1 7730488 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs12137936
rs12137936
NEGR1
2 1.000 0.040 1 72254674 intron variant C/G snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs12420205
rs12420205 		2 1.000 0.040 11 113523313 intergenic variant C/T snv 0.65 0.700 1.000 1 2018 2018
dbSNP: rs12457157
rs12457157
TCF4
2 1.000 0.040 18 55629696 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs1261070
rs1261070
TCF4
2 1.000 0.040 18 55235854 intron variant A/G snv 0.94 0.700 1.000 1 2018 2018
dbSNP: rs1261114
rs1261114
TCF4
2 1.000 0.040 18 55271138 intron variant G/A snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs12938775
rs12938775
PAFAH1B1
2 1.000 0.040 17 2671527 intron variant G/A;T snv 0.700 1.000 1 2018 2018