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: rs2835839
rs2835839
KCNJ6
3 1.000 0.080 21 37618732 3 prime UTR variant T/C snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs2835840
rs2835840
KCNJ6
3 1.000 0.080 21 37619019 3 prime UTR variant G/C snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs2835848
rs2835848
KCNJ6
3 1.000 0.080 21 37638771 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2835849
rs2835849
KCNJ6
3 1.000 0.080 21 37639222 intron variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs2835850
rs2835850
KCNJ6
3 1.000 0.080 21 37640675 intron variant T/C snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs2835852
rs2835852
KCNJ6
3 1.000 0.080 21 37641826 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs2835853
rs2835853
KCNJ6
3 1.000 0.080 21 37642590 intron variant C/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs2835855
rs2835855
KCNJ6
3 1.000 0.080 21 37643452 intron variant T/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs2835872
rs2835872
KCNJ6
3 1.000 0.080 21 37654970 intron variant G/A snv 0.26 0.800 1.000 1 2012 2012
dbSNP: rs2835880
rs2835880
KCNJ6
3 1.000 0.080 21 37660175 non coding transcript exon variant A/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs2835881
rs2835881
KCNJ6
3 1.000 0.080 21 37660829 non coding transcript exon variant G/A snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs2835888
rs2835888
KCNJ6
3 1.000 0.080 21 37677557 intron variant T/C snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs2835893
rs2835893
KCNJ6
3 1.000 0.080 21 37688590 intron variant G/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs2835894
rs2835894
KCNJ6
3 1.000 0.080 21 37693739 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs2835895
rs2835895
KCNJ6
3 1.000 0.080 21 37694050 intron variant C/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs2835896
rs2835896
KCNJ6
3 1.000 0.080 21 37694337 intron variant C/T snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs2835898
rs2835898
KCNJ6 ; LOC107985507
3 1.000 0.080 21 37699478 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2835900
rs2835900
KCNJ6 ; LOC107985507
3 1.000 0.080 21 37703447 intron variant G/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs2835910
rs2835910
KCNJ6 ; LOC107985507
3 1.000 0.080 21 37713604 intron variant C/T snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs3827195
rs3827195
KCNJ6
3 1.000 0.080 21 37677515 intron variant C/T snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs4452239
rs4452239
KCNJ6
3 1.000 0.080 21 37680353 intron variant T/G snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs4477996
rs4477996
KCNJ6
3 1.000 0.080 21 37680364 intron variant C/T snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs4816567
rs4816567
KCNJ6
3 1.000 0.080 21 37615853 3 prime UTR variant T/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs4816568
rs4816568
KCNJ6
3 1.000 0.080 21 37616044 3 prime UTR variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4817877
rs4817877
KCNJ6
3 1.000 0.080 21 37616091 3 prime UTR variant G/C snv 0.31 0.700 1.000 1 2012 2012