Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0025202
Disease: melanoma
melanoma
0.060 1.000 6 2010 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0025202
Disease: melanoma
melanoma
0.860 1.000 6 2010 2015
dbSNP: rs3219090
rs3219090
1.000 0.040 1 226376990 intron variant T/C snv 0.58
CUI: C0025202
Disease: melanoma
melanoma
0.820 1.000 2 2011 2013
dbSNP: rs45430
rs45430
MX2
1.000 0.040 21 41374154 intron variant C/T snv 0.48
CUI: C0025202
Disease: melanoma
melanoma
0.820 1.000 2 2011 2019
dbSNP: rs4911442
rs4911442
1.000 0.040 20 34767243 intron variant G/A snv 0.93
CUI: C0025202
Disease: melanoma
melanoma
0.720 1.000 2 2008 2014
dbSNP: rs10231520
rs10231520
1.000 0.040 7 20742471 intron variant C/T snv 0.29
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2013 2013
dbSNP: rs10515789
rs10515789
1.000 0.040 5 159079407 intron variant T/G snv 0.11
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2015 2015
dbSNP: rs10754833
rs10754833
0.851 0.040 1 236021631 intron variant T/A;C snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2011 2011
dbSNP: rs10757257
rs10757257
0.882 0.080 9 21806565 intron variant G/A snv 0.34
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 1 2009 2012
dbSNP: rs10830253
rs10830253
TYR
0.851 0.080 11 89294875 intron variant T/G snv 0.29
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2015 2015
dbSNP: rs10951982
rs10951982
0.851 0.160 7 6382925 intron variant G/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2018 2018
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2011 2011
dbSNP: rs1155563
rs1155563
GC
0.925 0.080 4 71777771 intron variant T/A;C snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2012 2012
dbSNP: rs12418451
rs12418451
0.882 0.080 11 69167951 intron variant G/A snv 0.22
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2015 2015
dbSNP: rs12621278
rs12621278
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2011 2011
dbSNP: rs132985
rs132985
0.827 0.120 22 38167464 intron variant C/T snv 0.51
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 1 2009 2012
dbSNP: rs1351383
rs1351383
1.000 0.040 6 32854492 intron variant A/C snv 0.43
CUI: C0025202
Disease: melanoma
melanoma
0.010 < 0.001 1 2013 2013
dbSNP: rs1544410
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2017 2017
dbSNP: rs1639679
rs1639679
1.000 0.040 7 140778454 intron variant G/T snv 9.8E-02
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2005 2005
dbSNP: rs16901979
rs16901979
0.724 0.480 8 127112671 intron variant C/A snv 0.16
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2011 2011
dbSNP: rs17817117
rs17817117
1.000 0.040 7 20685203 intron variant G/C snv 0.29
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2013 2013
dbSNP: rs187843643
rs187843643
1.000 0.040 5 17453974 intron variant C/T snv 3.9E-03
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 1 2017 2017
dbSNP: rs1990330
rs1990330
0.925 0.080 12 3038296 intron variant A/C;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2015 2015
dbSNP: rs2074560
rs2074560
MX2
0.925 0.040 21 41380411 intron variant A/G snv 0.43
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2014 2014
dbSNP: rs2107301
rs2107301
VDR
0.807 0.120 12 47861787 intron variant G/A snv 0.26
CUI: C0025202
Disease: melanoma
melanoma
0.010 < 0.001 1 2012 2012