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: rs10883437
rs10883437 		1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs17801127
rs17801127
MMADHC-DT
2 149707970 intron variant C/T snv 8.6E-02
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.800 1.000 1 2013 2013
dbSNP: rs2954021
rs2954021 		1.000 0.040 8 125469835 intron variant A/G snv 0.54
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs4949718
rs4949718
ST6GALNAC3
1 76433779 intron variant T/A;C snv
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.800 1.000 1 2013 2013
dbSNP: rs6834314
rs6834314 		0.807 0.160 4 87292656 intergenic variant A/G snv 0.24
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs738409
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.800 1.000 1 2011 2018