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: rs1928191
rs1928191 		6 39808584 intron variant C/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2395730
rs2395730 		6 39816589 intron variant C/A snv 0.58
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2010 2010
dbSNP: rs2395730
rs2395730 		6 39816589 intron variant C/A snv 0.58
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2010 2010
dbSNP: rs2395730
rs2395730 		6 39816589 intron variant C/A snv 0.58
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2010 2010
dbSNP: rs2504082
rs2504082 		6 39883903 non coding transcript exon variant A/G snv 0.45
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2504797
rs2504797 		6 39879503 non coding transcript exon variant G/A snv 0.16 0.12
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2504800
rs2504800 		6 39882522 intron variant T/C snv 0.63
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3003929
rs3003929 		6 39884042 synonymous variant G/A snv 0.60 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3003930
rs3003930 		6 39884261 non coding transcript exon variant T/C snv 0.53
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3003932
rs3003932 		6 39884662 non coding transcript exon variant A/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3003938
rs3003938 		6 39885414 non coding transcript exon variant A/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3003942
rs3003942 		6 39886649 non coding transcript exon variant A/G snv 0.68
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3004063
rs3004063 		6 39895441 intron variant A/G snv 0.67
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs2504106
rs2504106 		0.925 0.120 6 39854343 intron variant A/G snv 0.61
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2504106
rs2504106 		0.925 0.120 6 39854343 intron variant A/G snv 0.61
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs3004070
rs3004070 		1.000 0.040 6 39902176 3 prime UTR variant T/A snv 0.51
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease 		Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs6937133
rs6937133 		0.925 0.120 6 39832238 intron variant A/C;G snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs6937133
rs6937133 		0.925 0.120 6 39832238 intron variant A/C;G snv
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2009 2009