Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13009407
rs13009407
2 233743701 non coding transcript exon variant C/A;G;T snv 4.0E-06; 0.22; 4.0E-06
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs17864701
rs17864701
2 233744071 intron variant C/T snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs4663967
rs4663967
2 233744538 intron variant A/C snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs6741669
rs6741669
2 233744546 intron variant A/G snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013