Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7072216
rs7072216
PYROXD2 ; MIR1287
10 98397096 intron variant T/C snv 0.51
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2011 2013
dbSNP: rs1061437
rs1061437
HPS1 ; PYROXD2
10 98416397 3 prime UTR variant C/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10748729
rs10748729
PYROXD2
10 98411614 non coding transcript exon variant G/C snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10786415
rs10786415
PYROXD2
10 98391509 intron variant A/G snv 0.51
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10786418
rs10786418
PYROXD2
10 98397611 intron variant C/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10883084
rs10883084
PYROXD2
10 98391432 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10883085
rs10883085
PYROXD2 ; MIR1287
10 98395856 intron variant A/T snv 0.42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10883087
rs10883087
PYROXD2 ; MIR1287
10 98397233 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10883089
rs10883089
PYROXD2
10 98403363 intron variant A/C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10883092
rs10883092
PYROXD2
10 98407519 intron variant A/C snv 0.37
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11189586
rs11189586
PYROXD2
10 98394339 intron variant A/G snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11189590
rs11189590
PYROXD2 ; MIR1287
10 98394848 intron variant T/G snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11189592
rs11189592
PYROXD2 ; MIR1287
10 98395885 intron variant C/A snv 0.27
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11597425
rs11597425
PYROXD2
10 98394445 intron variant G/T snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11597428
rs11597428
PYROXD2
10 98394490 intron variant G/A;C snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs12763326
rs12763326
PYROXD2
10 98407639 synonymous variant G/A snv 0.32 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs12763379
rs12763379
PYROXD2
10 98407709 intron variant G/A snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17109605
rs17109605
PYROXD2
0.925 0.120 10 98385372 intron variant T/C snv 6.7E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs17109620
rs17109620
PYROXD2
10 98391181 intron variant G/A snv 5.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17109634
rs17109634
PYROXD2 ; MIR1287
1.000 0.040 10 98396036 intron variant C/T snv 5.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17109650
rs17109650
PYROXD2
10 98399616 intron variant T/C snv 5.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17109653
rs17109653
PYROXD2
10 98402394 intron variant T/C snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17109657
rs17109657
PYROXD2
10 98402938 intron variant G/C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17109662
rs17109662
PYROXD2
10 98406210 intron variant C/A snv 9.1E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17109675
rs17109675
PYROXD2
10 98408194 intron variant T/C snv 9.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013