Gene: DLGAP5 ×
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: rs2274273
rs2274273
DLGAP5
5 0.882 0.120 14 55147918 downstream gene variant G/A snv 0.40 0.800 1.000 1 2012 2012
dbSNP: rs10134800
rs10134800
DLGAP5
1 14 55168491 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134983
rs10134983
DLGAP5
1 14 55168605 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10140857
rs10140857
DLGAP5
1 14 55152893 intron variant G/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs10144326
rs10144326
DLGAP5
1 14 55177190 synonymous variant A/G snv 0.16 0.29 0.700 1.000 1 2012 2012
dbSNP: rs11622740
rs11622740
DLGAP5
1 14 55151126 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs15870
rs15870
DLGAP5
1 14 55152593 missense variant A/G;T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs2274271
rs2274271
DLGAP5
1 14 55188974 missense variant C/T snv 0.17 0.30 0.700 1.000 1 2012 2012
dbSNP: rs2296489
rs2296489
DLGAP5
1 14 55158259 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2340931
rs2340931
DLGAP5
1 14 55150219 intron variant T/G snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs3759667
rs3759667
DLGAP5 ; LOC105370508
1 14 55191703 upstream gene variant A/G snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs3818451
rs3818451
DLGAP5
1 14 55154398 intron variant C/G snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs6573007
rs6573007
DLGAP5
1 14 55159220 intron variant T/G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs6573008
rs6573008
DLGAP5
1 14 55188365 intron variant C/A snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs7159490
rs7159490
DLGAP5
1 14 55187691 intron variant C/T snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs7159808
rs7159808
DLGAP5
1 14 55157609 intron variant G/T snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs8003961
rs8003961
DLGAP5
1 14 55184835 intron variant A/G snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs8011834
rs8011834
DLGAP5
1 14 55159259 intron variant A/C snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs8018110
rs8018110
DLGAP5
1 14 55174996 intron variant C/T snv 0.57 0.700 1.000 1 2012 2012