Gene: ZNF407 ×
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: rs10221304
rs10221304
ZNF407
1 1.000 0.040 18 74669985 intron variant C/T snv 8.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs11151102
rs11151102
ZNF407
1 1.000 0.040 18 74661615 intron variant T/A snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs12458417
rs12458417
ZNF407
1 1.000 0.040 18 74668931 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs17055278
rs17055278
ZNF407
1 1.000 0.040 18 74637673 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs17055357
rs17055357
ZNF407
1 1.000 0.040 18 74669112 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs17817969
rs17817969
ZNF407
1 1.000 0.040 18 74632282 synonymous variant C/T snv 9.3E-02 0.11 0.700 1.000 1 2017 2017
dbSNP: rs3794941
rs3794941
ZNF407
1 1.000 0.040 18 74632267 synonymous variant T/C snv 0.15 0.20 0.700 1.000 1 2017 2017
dbSNP: rs488199
rs488199
ZNF407
1 1.000 0.040 18 74668190 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs520719
rs520719
ZNF407
1 1.000 0.040 18 74648959 intron variant T/C snv 0.10 0.700 1.000 1 2017 2017
dbSNP: rs574481
rs574481
ZNF407
1 1.000 0.040 18 74675179 intron variant G/A snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs8088980
rs8088980
ZNF407
3 1.000 0.040 18 74666435 intron variant C/T snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs948615
rs948615
ZNF407
1 1.000 0.040 18 74633934 missense variant A/C snv 0.15 0.20 0.700 1.000 1 2017 2017