Gene: TRPC4AP ×
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: rs10485508
rs10485508
TRPC4AP
2 20 35017295 intron variant C/T snv 8.0E-02 0.700 1.000 1 2010 2010
dbSNP: rs1058003
rs1058003
TRPC4AP ; MYH7B
2 20 35002614 3 prime UTR variant G/A snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs10875492
rs10875492
TRPC4AP
2 20 35043604 intron variant C/T snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs11696652
rs11696652
TRPC4AP
2 20 35049257 intron variant T/G snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs17092215
rs17092215
TRPC4AP
2 20 35008110 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs1885117
rs1885117
TRPC4AP
2 20 35012937 intron variant C/T snv 0.18 0.700 1.000 1 2010 2010
dbSNP: rs1885119
rs1885119
TRPC4AP
3 1.000 0.080 20 35057846 intron variant T/C snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs2145557
rs2145557
TRPC4AP
2 20 35079757 intron variant A/G snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs2378332
rs2378332
TRPC4AP
2 20 35029447 intron variant A/C;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2889873
rs2889873
TRPC4AP
2 20 35059038 intron variant G/A snv 8.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs3736802
rs3736802
TRPC4AP
3 1.000 0.080 20 35016239 intron variant T/C snv 0.53 0.700 1.000 1 2010 2010
dbSNP: rs3803937
rs3803937
TRPC4AP
2 20 35044884 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs3803938
rs3803938
TRPC4AP
2 20 35044797 intron variant C/T snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs3818253
rs3818253
TRPC4AP
3 1.000 0.040 20 35009073 intron variant G/A snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs4911460
rs4911460
TRPC4AP
2 20 35036527 intron variant G/A;C snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs6060151
rs6060151
TRPC4AP
2 20 35006423 intron variant G/T snv 0.65 0.58 0.700 1.000 1 2010 2010
dbSNP: rs6060162
rs6060162
TRPC4AP
2 20 35023658 intron variant C/G snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs6060170
rs6060170
TRPC4AP
2 20 35036663 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs6060172
rs6060172
TRPC4AP
2 20 35041002 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs6060216
rs6060216
TRPC4AP
2 20 35090275 intron variant T/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs6087660
rs6087660
TRPC4AP
2 20 35028725 intron variant T/C snv 0.59 0.700 1.000 1 2010 2010
dbSNP: rs6087664
rs6087664
TRPC4AP
3 1.000 0.080 20 35038413 intron variant C/A;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs6087666
rs6087666
TRPC4AP
2 20 35052439 intron variant G/A snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs6088678
rs6088678
TRPC4AP
2 20 35019748 intron variant C/T snv 0.18 0.700 1.000 1 2010 2010
dbSNP: rs6088686
rs6088686
TRPC4AP
2 20 35035634 intron variant C/T snv 0.19 0.700 1.000 1 2010 2010