Gene: SLC12A7 ×
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: rs35188965
rs35188965
SLC12A7
12 5 1104823 intron variant C/G;T snv 0.700 1.000 3 2016 2019
dbSNP: rs11133613
rs11133613
SLC12A7
2 5 1074936 intron variant A/G snv 0.91 0.700 1.000 2 2016 2017
dbSNP: rs111910553
rs111910553
SLC12A7
2 5 1058272 intron variant G/A snv 1.1E-02 0.700 1.000 2 2016 2017
dbSNP: rs187282666
rs187282666
SLC12A7
2 5 1093396 intron variant G/A snv 2.3E-03 0.700 1.000 2 2016 2017
dbSNP: rs112694389
rs112694389
SLC12A7
2 5 1067827 intron variant C/T snv 5.1E-04 0.700 1.000 1 2019 2019
dbSNP: rs11952124
rs11952124
SLC12A7
2 5 1076344 intron variant G/T snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs141839244
rs141839244
SLC12A7
2 5 1085619 intron variant C/T snv 8.9E-03 0.700 1.000 1 2016 2016
dbSNP: rs55861694
rs55861694
SLC12A7
2 5 1051642 3 prime UTR variant A/C snv 1.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs6883412
rs6883412
SLC12A7
2 5 1093746 intron variant C/G;T snv 0.700 1.000 1 2016 2016