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: rs10476781
rs10476781 		1 5 152384072 intron variant T/C snv 0.700 1.000 1 2018 2018
dbSNP: rs11213999
rs11213999
PPP2R1B
1 11 111763868 intron variant C/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs147672305
rs147672305
RIMS2
1 8 104058884 intron variant T/A snv 1.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs62047859
rs62047859 		1 16 76792494 intron variant T/A snv 1.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs78569750
rs78569750
CELF4
1 18 37278090 intron variant G/T snv 3.4E-02 0.700 1.000 1 2018 2018