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: rs10097731
rs10097731 		8 81115437 upstream gene variant G/T snv 0.12
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1260326
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs204999
rs204999 		0.763 0.480 6 32142202 intergenic variant A/G snv 0.28
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2280401
rs2280401
RPS11 ; SNORD35B
19 49496752 intron variant G/A snv 0.12
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3777200
rs3777200
ELL2
5 95899087 intron variant C/T snv 0.31
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4561508
rs4561508
TNFRSF13B
17 16945436 intron variant C/T snv 0.12
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0.700 1.000 1 2012 2012