SPRYD4, SPRY domain containing 4, 283377

N. diseases: 14; N. variants: 8
Disease: Serum albumin measurement ×
Source: ALL
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: rs1043011
rs1043011 		12 56471256 3 prime UTR variant G/T snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11171862
rs11171862 		12 56477530 3 prime UTR variant G/A snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2638314
rs2638314 		12 56472550 3 prime UTR variant T/A snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2638315
rs2638315 		12 56471272 3 prime UTR variant G/C snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2657879
rs2657879 		1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2657880
rs2657880 		12 56469986 3 prime UTR variant G/C snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7302925
rs7302925 		12 56467674 intron variant A/G snv 0.69
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012