Gene: GNG12-AS1 ×
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: rs12407028
rs12407028
WLS ; GNG12-AS1
2 1 68182033 intron variant T/A;C snv 0.35 0.800 1.000 2 2009 2012
dbSNP: rs1430740
rs1430740
WLS ; GNG12-AS1
2 1 68191827 intron variant T/C snv 0.58 0.800 1.000 2 2009 2014
dbSNP: rs1430742
rs1430742
WLS ; GNG12-AS1
1 1 68169392 intron variant T/C snv 0.18 0.800 1.000 1 2009 2009
dbSNP: rs2566755
rs2566755
WLS ; GNG12-AS1
1 1 68169707 intron variant T/C snv 0.19 0.800 1.000 1 2009 2009
dbSNP: rs1036066
rs1036066
WLS ; GNG12-AS1
1 1 68194522 intron variant A/C snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs12568456
rs12568456
WLS ; GNG12-AS1
1 1 68195803 intron variant T/G snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs12733835
rs12733835
WLS ; GNG12-AS1
1 1 68157311 intron variant C/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs1367447
rs1367447
WLS ; GNG12-AS1
1 1 68168347 intron variant C/T snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs17130567
rs17130567
WLS ; GNG12-AS1
1 1 68198164 intron variant A/G snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs2039154
rs2039154
WLS ; GNG12-AS1
1 1 68197130 intron variant G/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs2116046
rs2116046
WLS ; GNG12-AS1
1 1 68196569 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2116047
rs2116047
WLS ; GNG12-AS1
1 1 68196068 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2195682
rs2195682
WLS ; GNG12-AS1
1 1 68170060 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2566752
rs2566752
WLS ; GNG12-AS1
2 1.000 0.080 1 68191014 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs2566754
rs2566754
WLS ; GNG12-AS1
1 1 68175555 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs2566758
rs2566758
WLS ; GNG12-AS1
1 1 68166800 intron variant C/T snv 0.54 0.700 1.000 1 2009 2009
dbSNP: rs2566759
rs2566759
WLS ; GNG12-AS1
1 1 68166109 intron variant G/A snv 0.53 0.700 1.000 1 2009 2009
dbSNP: rs2566784
rs2566784
WLS ; GNG12-AS1
1 1 68137052 intron variant G/T snv 0.26 0.700 1.000 1 2009 2009
dbSNP: rs2772300
rs2772300
WLS ; GNG12-AS1
1 1 68182343 intron variant G/A snv 0.23 0.700 1.000 1 2009 2009
dbSNP: rs2772304
rs2772304
WLS ; GNG12-AS1
1 1 68170897 intron variant C/A snv 0.27 0.700 1.000 1 2009 2009
dbSNP: rs2820500
rs2820500
WLS ; GNG12-AS1
1 1 68193278 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs3762371
rs3762371
WLS ; GNG12-AS1
1 1 68155079 intron variant G/A snv 0.36 0.34 0.700 1.000 1 2009 2009
dbSNP: rs4233320
rs4233320
WLS ; GNG12-AS1
1 1 68172768 intron variant G/T snv 0.39 0.700 1.000 1 2009 2009
dbSNP: rs6677666
rs6677666
WLS ; GNG12-AS1
1 1 68174418 intron variant C/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs7554551
rs7554551
WLS ; GNG12-AS1
1 1 68199340 intron variant T/C;G snv 0.700 1.000 1 2009 2009