Source: GWASCAT

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: rs6040076
rs6040076
20 10678234 intron variant G/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 2 2016 2019
dbSNP: rs9883204
rs9883204
3 123377973 intron variant T/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.800 1.000 2 2010 2013
dbSNP: rs10173538
rs10173538
2 159712765 intron variant C/G;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs10283100
rs10283100
8 119583783 missense variant A/G;T snv 0.96
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs10495563
rs10495563
2 9522081 3 prime UTR variant G/A;C;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs11055034
rs11055034
1.000 0.080 12 12737692 intron variant C/A;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2016 2016
dbSNP: rs11082304
rs11082304
18 23141009 intron variant G/C;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs113086489
rs113086489
17 7268037 upstream gene variant C/A;G;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2016 2016
dbSNP: rs116964396
rs116964396
8 41648330 intron variant C/A;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs11698914
rs11698914
20 32739337 intron variant C/A;G snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs11711420
rs11711420
3 183631222 upstream gene variant T/A;G snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs11765649
rs11765649
7 23439394 intron variant T/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2016 2016
dbSNP: rs1179494
rs1179494
2 36582353 intron variant G/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs11867479
rs11867479
17 70094066 intron variant C/A;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs11957761
rs11957761
5 141678920 intron variant G/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs1242516
rs1242516
17 17483765 intron variant T/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs12443252
rs12443252
15 90521458 intergenic variant C/A;G;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs12623454
rs12623454
2 120568721 intergenic variant G/C;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs12896104
rs12896104
14 73839311 downstream gene variant A/G;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs12942207
rs12942207
17 47890928 downstream gene variant C/A;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2016 2016
dbSNP: rs1323438
rs1323438
9 116353252 intron variant T/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs1351394
rs1351394
12 65958046 3 prime UTR variant T/C;G snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2016 2016
dbSNP: rs144843919
rs144843919
17 30710321 intron variant G/A;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2016 2016
dbSNP: rs1547669
rs1547669
6 33807864 upstream gene variant A/G;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs1819436
rs1819436
13 78006148 intron variant T/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2016 2016