Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1787394
KCNJ6
1.000 0.080 21 37663874 intron variant C/A snv 0.58 3
rs1787395
KCNJ6
1.000 0.080 21 37664176 intron variant A/C;T snv 3
rs1787396
KCNJ6
1.000 0.080 21 37664185 intron variant A/C snv 0.57 3
rs1787397
KCNJ6
1.000 0.080 21 37665076 intron variant A/G snv 0.57 3
rs1787398
KCNJ6
1.000 0.080 21 37665202 intron variant A/C snv 0.57 3
rs1787399
KCNJ6
1.000 0.080 21 37665581 intron variant A/G snv 0.57 3
rs1787400
KCNJ6
1.000 0.080 21 37665915 intron variant G/C snv 0.57 3
rs1787401
KCNJ6
1.000 0.080 21 37666591 intron variant C/G;T snv 3
rs1787402
KCNJ6
1.000 0.080 21 37666688 intron variant C/A;G;T snv 3
rs1787404
KCNJ6
1.000 0.080 21 37677060 intron variant A/C;G snv 3
rs1787406
KCNJ6
1.000 0.080 21 37678866 intron variant C/A snv 0.50 3
rs1888467
KCNJ6
1.000 0.080 21 37680478 intron variant G/T snv 0.47 3
rs2154553
KCNJ6
1.000 0.080 21 37632199 intron variant G/A;T snv 0.71 3
rs2835831
KCNJ6
1.000 0.080 21 37614931 3 prime UTR variant T/C snv 0.29 3
rs2835833
KCNJ6
1.000 0.080 21 37615595 3 prime UTR variant G/A;C snv 0.31 3
rs2835835
KCNJ6
1.000 0.080 21 37616770 3 prime UTR variant G/A snv 0.32 3
rs2835836
KCNJ6
1.000 0.080 21 37616885 3 prime UTR variant A/C snv 0.26 3
rs2835837
KCNJ6
1.000 0.080 21 37618141 3 prime UTR variant G/A snv 0.30 3
rs2835838
KCNJ6
1.000 0.080 21 37618692 3 prime UTR variant A/G snv 0.32 3
rs2835839
KCNJ6
1.000 0.080 21 37618732 3 prime UTR variant T/C snv 0.25 3
rs2835840
KCNJ6
1.000 0.080 21 37619019 3 prime UTR variant G/C snv 0.30 3
rs2835848
KCNJ6
1.000 0.080 21 37638771 intron variant C/G;T snv 3
rs2835849
KCNJ6
1.000 0.080 21 37639222 intron variant T/C snv 0.27 3
rs2835850
KCNJ6
1.000 0.080 21 37640675 intron variant T/C snv 0.25 3
rs2835852
KCNJ6
1.000 0.080 21 37641826 intron variant G/A snv 0.27 3