Source: BEFREE

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: rs75002628
rs75002628
ALB
0.925 0.080 4 73412007 missense variant G/A;C snv 7.2E-05
CUI: C0342185
Disease: Hyperthyroxinemia, Familial Dysalbuminemic
Hyperthyroxinemia, Familial Dysalbuminemic 		0.820 1.000 2 1994 2019
dbSNP: rs374651285
rs374651285
ALB
4 73406645 missense variant G/A snv
CUI: C0027765
Disease: nervous system disorder
nervous system disorder 		0.010 1.000 1 2019 2019
dbSNP: rs75002628
rs75002628
ALB
0.925 0.080 4 73412007 missense variant G/A;C snv 7.2E-05
CUI: C0020551
Disease: Hyperthyroxinemia
Hyperthyroxinemia 		0.010 1.000 1 2019 2019