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: rs498475
rs498475
JAZF1-AS1
1 7 28216621 intron variant G/A snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs56317999
rs56317999
DSN1
1 20 36757832 intron variant G/A snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs569557
rs569557
F7
1 13 113115603 intron variant G/A snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs6083120
rs6083120
NAPB
1 20 23415361 intron variant C/T snv 8.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs6119569
rs6119569
TRPC4AP
1 20 35084568 intron variant G/A snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs6532796
rs6532796
LOC100507053
2 1.000 0.040 4 99121091 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs71446935
rs71446935
MCF2L
1 13 113080062 intron variant A/G snv 0.700 1.000 1 2019 2019
dbSNP: rs72873804
rs72873804 		1 18 5947039 intron variant G/C;T snv 4.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs7935829
rs7935829
MS4A6A
3 1.000 0.080 11 60175342 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs7946992
rs7946992
MS4A6A
1 11 60177337 non coding transcript exon variant T/C snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs9805933
rs9805933 		1 14 44551736 intron variant A/C snv 0.32 0.700 1.000 1 2019 2019