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: rs4663333
rs4663333
3 2 233746657 intron variant G/T snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs4663963
rs4663963
3 2 233741547 non coding transcript exon variant T/G snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs4663965
rs4663965
3 2 233741958 intron variant T/C snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs4663967
rs4663967
3 2 233744538 intron variant A/C snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs4663971
rs4663971
3 2 233765606 intron variant C/G;T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs6431628
rs6431628
3 2 233738832 intron variant A/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs6714634
rs6714634
4 2 233756119 non coding transcript exon variant T/C snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs6715325
rs6715325
3 2 233726595 intron variant T/C snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs6741669
rs6741669
3 2 233744546 intron variant A/G snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs6742078
rs6742078
13 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs6747843
rs6747843
3 2 233755708 non coding transcript exon variant G/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs7564935
rs7564935
3 2 233736540 intron variant G/T snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs7574296
rs7574296
3 2 233729603 synonymous variant A/G snv 0.49 0.54 0.700 1.000 1 2013 2013
dbSNP: rs7597496
rs7597496
3 2 233721797 non coding transcript exon variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs7604115
rs7604115
4 2 233749470 intron variant C/T snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs869283
rs869283
3 2 233717641 intron variant G/A snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs871514
rs871514
3 2 233719883 intron variant T/C snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs929596
rs929596
9 0.925 0.040 2 233765830 intron variant A/G snv 0.32 0.700 1.000 1 2013 2013