Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121913513
rs121913513
0.776 0.120 4 54727495 missense variant T/C snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.760 1.000 17 1995 2016
dbSNP: rs1057519710
rs1057519710
0.695 0.280 4 54733166 missense variant G/C;T snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.710 1.000 10 1995 2013
dbSNP: rs121913517
rs121913517
0.851 0.120 4 54727444 missense variant T/A;C;G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 18 1995 2014
dbSNP: rs121913235
rs121913235
0.925 0.080 4 54727437 missense variant T/A;C;G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 14 1995 2012
dbSNP: rs121913512
rs121913512
0.851 0.120 4 54728055 missense variant A/C;G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 9 1995 2011
dbSNP: rs121913506
rs121913506
0.677 0.320 4 54733154 missense variant G/A;C;T snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 8 1995 2011
dbSNP: rs1057519708
rs1057519708
1.000 0.040 4 54728096 missense variant T/A;G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 3 2011 2014
dbSNP: rs1057519703
rs1057519703
1.000 0.040 4 54727418 missense variant A/C;T snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 2 2014 2014
dbSNP: rs1057519704
rs1057519704
0.882 0.080 4 54727425 missense variant T/A snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 2 2011 2012
dbSNP: rs1057519705
rs1057519705
1.000 0.040 4 54727464 missense variant A/G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 2 2014 2014
dbSNP: rs1057519706
rs1057519706
1.000 0.040 4 54727474 missense variant T/G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 2 2014 2014
dbSNP: rs121913514
rs121913514
0.763 0.240 4 54733174 missense variant T/A;G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 2 2011 2012
dbSNP: rs121913521
rs121913521
0.790 0.120 4 54727447 missense variant T/A;C;G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 2 2008 2014
dbSNP: rs121913523
rs121913523
1.000 0.040 4 54728092 missense variant T/A;C snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 2 2011 2012
dbSNP: rs1057519702
rs1057519702
1.000 0.040 4 54726020 missense variant T/C snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs1057519713
rs1057519713
0.925 0.120 4 54736498 missense variant G/C snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 1 2013 2013
dbSNP: rs121913524
rs121913524
1.000 0.040 4 54733182 missense variant T/C snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs121913685
rs121913685
0.882 0.080 4 54727443 inframe deletion TTGTTG/-;TTG delins
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs200375589
rs200375589
1.000 0.040 4 54727442 missense variant G/A;C;T snv 6.0E-05
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 1 2012 2012
dbSNP: rs993022333
rs993022333
0.851 0.080 4 54733173 missense variant A/C;T snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs1057520031
rs1057520031
1.000 0.040 4 54727440 missense variant A/C;G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs1060502550
rs1060502550
1.000 0.040 4 54727488 missense variant A/G snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 < 0.001 1 2011 2011
dbSNP: rs2237028
rs2237028
1.000 0.040 4 54670209 intron variant T/G snv 0.44
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2013 2013