Gene: SMARCA4 ×
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: rs112374545
rs112374545
SMARCA4
2 19 11078223 intron variant C/T snv 0.11 0.700 1.000 3 2015 2019
dbSNP: rs143020224
rs143020224
SMARCA4
2 19 11076648 intron variant C/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs73015011
rs73015011
SMARCA4
2 19 11079088 missense variant T/C snv 0.13 0.700 1.000 2 2018 2019
dbSNP: rs1122608
rs1122608
SMARCA4
16 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs11669133
rs11669133
SMARCA4
2 1.000 0.040 19 10981463 intron variant G/A snv 4.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs12052201
rs12052201
SMARCA4
2 19 11048420 intron variant G/T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs1529729
rs1529729
SMARCA4
3 19 11052886 intron variant C/T snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs17001095
rs17001095
SMARCA4
2 19 11022596 intron variant A/G snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs3786722
rs3786722
SMARCA4
2 19 11050861 intron variant C/A snv 0.18 0.700 1.000 1 2018 2018