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: rs900400
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 2 2010 2013
dbSNP: rs9883204
rs9883204
ADCY5
3 123377973 intron variant T/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 2 2010 2013
dbSNP: rs1042725
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2013 2013
dbSNP: rs12340987
rs12340987 		9 85156012 upstream gene variant A/G snv 0.19
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2014 2014
dbSNP: rs1801253
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2013 2019
dbSNP: rs4432842
rs4432842 		1.000 0.080 5 57876251 intergenic variant T/C snv 0.45
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2013 2013
dbSNP: rs6931514
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2013 2013
dbSNP: rs724577
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2013 2013
dbSNP: rs7780752
rs7780752
GNGT1
7 93612328 intron variant T/C snv 0.27
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2013 2013
dbSNP: rs10788038
rs10788038 		10 120117008 intergenic variant T/C snv 0.61
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2007 2007
dbSNP: rs2960051
rs2960051 		18 30276169 intergenic variant C/T snv 0.84
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2007 2007
dbSNP: rs3107997
rs3107997
LOC105372046 ; LOC105372047
18 30340278 intron variant C/T snv 0.21
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2007 2007
dbSNP: rs4564656
rs4564656 		18 30301067 intron variant G/A snv 0.76
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2007 2007
dbSNP: rs6508654
rs6508654 		18 30302598 intron variant T/C snv 0.81
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2007 2007
dbSNP: rs7849941
rs7849941
LOC107987088
9 85130318 intergenic variant A/T snv 0.27
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2014 2014