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: rs10807187
rs10807187
MDGA1
1 1.000 0.040 6 37661874 intron variant G/A;T snv 0.35 0.010 1.000 1 2011 2011
dbSNP: rs10821736
rs10821736
ANK3
1 1.000 0.040 10 60345295 intron variant C/T snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs10821745
rs10821745
ANK3
1 1.000 0.040 10 60376448 intron variant T/G snv 9.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs10821748
rs10821748
ANK3
1 1.000 0.040 10 60393180 intron variant G/C snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs10821789
rs10821789
ANK3
1 1.000 0.040 10 60525580 intron variant G/A snv 9.2E-02 0.700 1.000 1 2014 2014
dbSNP: rs10821792
rs10821792
ANK3
1 1.000 0.040 10 60538858 intron variant C/T snv 8.3E-02 0.700 1.000 1 2014 2014
dbSNP: rs10848632
rs10848632
CACNA1C
1 1.000 0.040 12 2206827 intron variant C/T snv 0.34 0.010 1.000 1 2019 2019
dbSNP: rs10848642
rs10848642
CACNA1C ; CACNA1C-AS4
1 1.000 0.040 12 2222406 non coding transcript exon variant A/G snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs10852173
rs10852173 		1 1.000 0.040 15 92379618 intergenic variant A/T snv 0.68 0.010 1.000 1 2015 2015
dbSNP: rs10878840
rs10878840 		1 1.000 0.040 12 68487269 upstream gene variant G/A snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs10884920
rs10884920
ADD3
1 1.000 0.040 10 110015049 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10889182
rs10889182
LINC01748
1 1.000 0.040 1 60532523 intron variant T/G snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs10889187
rs10889187
LINC01748
1 1.000 0.040 1 60545086 intron variant G/A snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs10889189
rs10889189
LINC01748
1 1.000 0.040 1 60559354 intron variant C/G snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs10896090
rs10896090
PACS1
1 1.000 0.040 11 66177715 intron variant A/G snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs10994299
rs10994299
ANK3
1 1.000 0.040 10 60316870 intron variant C/A snv 6.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs10994308
rs10994308
ANK3
1 1.000 0.040 10 60339194 intron variant G/A snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs10994322
rs10994322
ANK3
1 1.000 0.040 10 60376521 intron variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs10994404
rs10994404
ANK3
1 1.000 0.040 10 60528687 intron variant T/C;G snv 0.700 1.000 1 2014 2014
dbSNP: rs10994415
rs10994415
ANK3
1 1.000 0.040 10 60562276 intron variant T/C snv 8.7E-02 0.800 1.000 1 2014 2014
dbSNP: rs10994429
rs10994429
ANK3
1 1.000 0.040 10 60611321 intron variant C/T snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs10994430
rs10994430
ANK3
1 1.000 0.040 10 60612195 intron variant G/T snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs11129735
rs11129735
TRANK1
1 1.000 0.040 3 36828739 intron variant A/G snv 0.53 0.700 1.000 1 2014 2014
dbSNP: rs11178998
rs11178998
TPH2
1 1.000 0.040 12 71938935 5 prime UTR variant A/G snv 5.7E-02 0.010 1.000 1 2016 2016
dbSNP: rs11207633
rs11207633
LINC01748
1 1.000 0.040 1 60541510 non coding transcript exon variant A/G snv 0.32 0.700 1.000 1 2013 2013