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: rs7200543
rs7200543 		16 15036113 synonymous variant A/G snv 0.35 0.30
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2017 2018
dbSNP: rs3198697
rs3198697 		16 15036083 missense variant C/A;T snv 4.0E-06; 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2013 2018
dbSNP: rs4985155
rs4985155 		16 15035602 intron variant A/G snv 0.40 0.37
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2015 2019
dbSNP: rs11075253
rs11075253 		16 15054789 intron variant C/A snv 0.22
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs1136001
rs1136001 		16 15038117 missense variant G/A;T snv 4.0E-06; 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11376559
rs11376559 		16 15037797 3 prime UTR variant -/A;AA;AAA delins
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2017 2017
dbSNP: rs11644601
rs11644601 		16 15078261 intron variant T/C snv 0.21
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11644601
rs11644601 		16 15078261 intron variant T/C snv 0.21
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11644601
rs11644601 		16 15078261 intron variant T/C snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11644601
rs11644601 		16 15078261 intron variant T/C snv 0.21
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12928099
rs12928099 		16 15056648 intron variant C/A snv 0.20
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12928099
rs12928099 		16 15056648 intron variant C/A snv 0.20
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs14347
rs14347 		16 15040032 synonymous variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16966953
rs16966953 		16 15041997 intron variant A/G snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1741
rs1741 		16 15036494 3 prime UTR variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2740
rs2740 		16 15038251 3 prime UTR variant A/C;G snv 0.33
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3198697
rs3198697 		16 15036083 missense variant C/A;T snv 4.0E-06; 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34614532
rs34614532 		16 15039051 intron variant T/C snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34614532
rs34614532 		16 15039051 intron variant T/C snv 0.30
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs34955778
rs34955778 		16 15045737 non coding transcript exon variant T/C snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35811052
rs35811052 		16 15034559 splice region variant A/G snv 0.25 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3803573
rs3803573 		16 15044556 non coding transcript exon variant C/T snv 0.29
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs4122352
rs4122352 		16 15080714 intron variant G/A snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4500751
rs4500751 		16 15046354 intron variant C/T snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 1.000 1 2012 2012
dbSNP: rs4985124
rs4985124 		16 15031584 intron variant T/G snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012