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: rs2294239
rs2294239
ZNRF3
4 22 29053489 intron variant A/G snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs2047937
rs2047937
ZNF423
5 0.925 0.120 16 49830880 intron variant C/T snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs7506051
rs7506051
ZNF407
1 18 74589381 downstream gene variant A/C snv 0.72 0.700 1.000 1 2010 2010
dbSNP: rs17657696
rs17657696
ZNF285
2 19 44401857 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs905938
rs905938
ZBTB7B ; DCST2
5 1 155018913 intron variant T/C snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs1344674
rs1344674
ZBTB38
4 3 141406344 intron variant A/G snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs55883249
rs55883249
YWHAQ
2 2 9601406 intron variant C/A snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs57827131
rs57827131
XXYLT1
2 3 195192301 intron variant A/T snv 9.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs113496184
rs113496184
WWOX
2 16 79006207 intron variant G/C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs4720530
rs4720530
WIPI2
3 7 5212643 intron variant C/T snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs2645294
rs2645294
WARS2
4 1 119031964 3 prime UTR variant C/T snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs76124550
rs76124550
VTI1A
2 10 112626980 intron variant C/T snv 2.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs3102841
rs3102841
VIRMA
1 8 94506977 intron variant C/A snv 0.56 0.700 1.000 1 2010 2010
dbSNP: rs115219852
rs115219852
USP34
2 2 61424393 intron variant G/A snv 2.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs180850064
rs180850064
UBAP2
2 9 33995448 non coding transcript exon variant A/G snv 1.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs79546472
rs79546472
U2AF2
2 19 55662011 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs9924009
rs9924009
TXNDC11
2 16 11688193 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs61571577
rs61571577
TTC7A
2 2 47009297 intron variant C/T snv 5.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs2274432
rs2274432
TSEN15
5 1 184051811 missense variant G/A snv 0.33 0.28 0.700 1.000 1 2017 2017
dbSNP: rs2309891
rs2309891
TRPM3
2 9 71226002 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs10031466
rs10031466
TRIML2
2 4 188094248 intron variant G/A snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs75755010
rs75755010
TRAPPC9
2 8 139983697 intron variant G/A snv 6.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs10501157
rs10501157
TRAF6
2 11 36485319 3 prime UTR variant T/C snv 1.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs114951929
rs114951929
TNK2
2 3 195864852 intron variant G/A snv 5.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs150394119
rs150394119
TNIK
2 3 171403444 intron variant G/A snv 6.2E-02 0.700 1.000 1 2015 2015