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: rs2227885
rs2227885
GJA1
2 0.925 0.080 6 121447932 missense variant G/A snv 4.2E-04 1.3E-04 0.800 0
dbSNP: rs104893965
rs104893965
GJA1
2 0.925 0.080 6 121447974 missense variant G/A snv 2.0E-04 1.8E-04 0.700 1.000 1 2001 2001
dbSNP: rs11008222
rs11008222 		2 0.925 0.080 10 30753565 intergenic variant G/A snv 0.39 0.700 1.000 1 2015 2015
dbSNP: rs11894932
rs11894932
MGAT4A
2 0.925 0.080 2 98648723 intron variant A/C snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs12045807
rs12045807
ENSA
2 0.925 0.080 1 150612358 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs1642645
rs1642645
HIVEP3
2 0.925 0.080 1 42036610 intron variant A/C snv 0.80 0.700 1.000 1 2017 2017
dbSNP: rs1975649
rs1975649
SYNPR ; SYNPR-AS1
2 0.925 0.080 3 63453210 intron variant T/C snv 0.74 0.700 1.000 1 2015 2015
dbSNP: rs3746446
rs3746446
MYH7B
2 0.925 0.080 20 34986962 synonymous variant T/C snv 0.19 0.18 0.700 1.000 1 2016 2016
dbSNP: rs55788414
rs55788414
PKD1L2
2 0.925 0.080 16 81151334 intron variant C/T snv 6.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs72820264
rs72820264
HULC
2 0.925 0.080 6 9291650 intron variant T/C snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs77471149
rs77471149 		2 0.925 0.080 4 167914184 intergenic variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs8061121
rs8061121
C16orf95
2 0.925 0.080 16 87159478 intron variant T/C snv 0.89 0.700 1.000 1 2015 2015