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: rs7587476
rs7587476
BARD1
1 1.000 0.040 2 214789163 intron variant T/A;C snv 0.800 1.000 2 2009 2012
dbSNP: rs10131293
rs10131293
LOC105370401
1 1.000 0.040 14 22461166 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs10132733
rs10132733
LOC105370401 ; LOC112267867
1 1.000 0.040 14 22477241 intron variant A/G snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs10142552
rs10142552
LOC105370401
1 1.000 0.040 14 22395232 intron variant G/A snv 3.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10148895
rs10148895 		1 1.000 0.040 14 22254840 intron variant C/T snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs10155916
rs10155916
LOC107986784
1 1.000 0.040 7 38286177 intergenic variant G/A snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs10162417
rs10162417
LOC105370401
1 1.000 0.040 14 22460708 intron variant T/G snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs1040303
rs1040303
LOC105370401
1 1.000 0.040 14 22403377 intron variant G/A snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10441090
rs10441090 		1 1.000 0.040 7 38295217 upstream gene variant C/T snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10483273
rs10483273
LOC105370401
1 1.000 0.040 14 22448054 intron variant A/G snv 9.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10483275
rs10483275
TRDC ; LOC105370401 ; LOC112267867
1 1.000 0.040 14 22464064 intron variant C/T snv 9.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10483277
rs10483277
LOC105370401 ; LOC112267867
1 1.000 0.040 14 22471852 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10487742
rs10487742 		1 1.000 0.040 7 38326911 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs10742682
rs10742682
HSD17B12
1 1.000 0.040 11 43644307 non coding transcript exon variant C/T snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs1076861
rs1076861
LOC105370401 ; LOC112267867
1 1.000 0.040 14 22473629 intron variant G/A snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs10932572
rs10932572
BARD1
1 1.000 0.040 2 214762673 intron variant A/G snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs11157596
rs11157596
LOC105370401
1 1.000 0.040 14 22438076 intron variant G/A snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs11579261
rs11579261 		1 1.000 0.040 1 143544453 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11587304
rs11587304 		1 1.000 0.040 1 143653074 upstream gene variant A/C snv 0.83 0.700 1.000 1 2009 2009
dbSNP: rs11623995
rs11623995
LOC105370401
1 1.000 0.040 14 22436733 intron variant A/G snv 0.74 0.700 1.000 1 2009 2009
dbSNP: rs11624054
rs11624054
LOC105370401
1 1.000 0.040 14 22406085 intron variant A/G snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs11765884
rs11765884
TRGV9
1 1.000 0.040 7 38317722 5 prime UTR variant C/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs11769443
rs11769443
TRGV9
1 1.000 0.040 7 38317474 missense variant T/C snv 0.39 0.42 0.700 1.000 1 2009 2009
dbSNP: rs11848747
rs11848747
LOC105370401
1 1.000 0.040 14 22452288 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11975431
rs11975431 		1 1.000 0.040 7 38322024 upstream gene variant C/T snv 0.14 0.700 1.000 1 2009 2009