Gene: TNFSF8 ×
Source: GWASDB ×
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: rs1322054
rs1322054
TNFSF8 ; DELEC1
1 1.000 0.040 9 114907019 intron variant A/G snv 0.58 0.700 1.000 1 2005 2005
dbSNP: rs1885383
rs1885383
TNFSF8 ; DELEC1
1 1.000 0.040 9 114917522 intron variant G/A snv 0.21 0.700 1.000 1 2005 2005
dbSNP: rs2295800
rs2295800
TNFSF8 ; DELEC1
1 1.000 0.040 9 114901931 intron variant T/C snv 0.56 0.700 1.000 1 2005 2005
dbSNP: rs2974
rs2974
TNFSF8 ; DELEC1
1 1.000 0.040 9 114901892 intron variant T/C snv 0.56 0.700 1.000 1 2005 2005
dbSNP: rs3181360
rs3181360
TNFSF8 ; DELEC1
1 1.000 0.040 9 114929278 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs3181362
rs3181362
TNFSF8 ; DELEC1
1 1.000 0.040 9 114905163 intron variant T/C snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs3789879
rs3789879
TNFSF8 ; DELEC1
1 1.000 0.040 9 114915956 intron variant T/C snv 0.58 0.700 1.000 1 2005 2005
dbSNP: rs3789882
rs3789882
TNFSF8 ; DELEC1
1 1.000 0.040 9 114907419 intron variant A/T snv 0.22 0.700 1.000 1 2005 2005