Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9892942
FAM222B
17 28851743 intron variant C/T snv 0.25 4
rs9914988
ERAL1 ; FAM222B
17 28856086 intron variant G/A snv 0.74 2
rs12946844
FAM222B
17 28843138 intron variant C/G;T snv 2
rs35033748
FAM222B
17 28852572 intron variant T/C snv 0.26 2
rs7215310
FAM222B
17 28761608 intron variant C/A snv 0.19 2
rs1035989
FAM222B
17 28816792 intron variant T/A;G snv 1
rs11650788
FAM222B
17 28847505 intron variant T/A snv 0.25 1
rs11652272
FAM222B
17 28840955 intron variant C/G snv 0.19 1
rs11658884
FAM222B
17 28805724 intron variant G/A snv 0.19 1
rs12453504
FAM222B
17 28792506 intron variant C/A;T snv 1
rs17721223
FAM222B
17 28839688 intron variant A/T snv 2.5E-02 1
rs2043031
FAM222B
17 28758546 synonymous variant A/G snv 0.21 0.19 1
rs2043032
FAM222B
17 28809674 intron variant A/G snv 0.19 1
rs2046759
FAM222B
17 28811799 intron variant T/C snv 0.19 1
rs28847895
FAM222B
17 28845502 intron variant T/C;G snv 0.26 1
rs4794836
FAM222B
17 28755692 downstream gene variant C/G snv 0.29 1
rs4795457
FAM222B
17 28760911 intron variant C/T snv 0.19 1
rs4795459
FAM222B
17 28786708 intron variant G/C;T snv 0.19 1
rs4795463
FAM222B
17 28819371 intron variant G/C snv 0.19 1
rs4795464
FAM222B
17 28819479 intron variant G/C snv 0.19 1
rs4795465
FAM222B
17 28824480 intron variant C/T snv 0.19 1
rs57583458
FAM222B
17 28779752 intron variant TAAATAAATAAATAAATAAATAAATAAA/-;TAAATAAATAAA;TAAATAAATAAATAAA;TAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAATAAATAAA delins 1
rs7215000
FAM222B
17 28761418 intron variant C/A;T snv 1
rs8078402
FAM222B
17 28818106 intron variant T/A snv 0.19 1
rs9303621
FAM222B
17 28834120 intron variant A/G snv 0.19 1