Source: BEFREE ×
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: rs4662344
rs4662344
ARHGAP15
3 0.925 0.080 2 143591289 intron variant T/C snv 0.82 0.710 1.000 1 2017 2017
dbSNP: rs67153654
rs67153654
FAM155A
3 0.925 0.080 13 107572636 intron variant T/A;C snv 0.710 1.000 1 2017 2017
dbSNP: rs7609897
rs7609897
COLQ
3 0.925 0.080 3 15461174 intron variant G/T snv 0.22 0.710 1.000 1 2017 2017
dbSNP: rs7848647
rs7848647
TNFSF15
11 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 0.020 1.000 2 2014 2017
dbSNP: rs4263839
rs4263839
TNFSF15
5 0.807 0.160 9 114804160 intron variant A/G snv 0.75 0.010 1.000 1 2017 2017
dbSNP: rs6478108
rs6478108
TNFSF15
10 0.763 0.200 9 114796423 intron variant C/T snv 0.73 0.010 1.000 1 2017 2017
dbSNP: rs6478109
rs6478109
TNFSF15
11 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2017 2017
dbSNP: rs7869487
rs7869487 		3 0.882 0.040 9 114818634 intergenic variant C/G;T snv 0.010 1.000 1 2017 2017