Source: ALL

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: rs8026235
rs8026235
15 88806225 intron variant A/C snv 1.7E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2280470
rs2280470
15 88852395 intron variant A/G snv 0.68
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2010 2017
dbSNP: rs2280470
rs2280470
15 88852395 intron variant A/G snv 0.68
CUI: C0489786
Disease: Height
Height
0.700 1.000 2 2010 2013
dbSNP: rs8042988
rs8042988
15 88869048 intron variant A/G snv 0.43
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2014 2019
dbSNP: rs11630187
rs11630187
15 88844673 intron variant A/G snv 0.78
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs16942333
rs16942333
15 88845033 intron variant A/G snv 3.3E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16942333
rs16942333
15 88845033 intron variant A/G snv 3.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16942333
rs16942333
15 88845033 intron variant A/G snv 3.3E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2280470
rs2280470
15 88852395 intron variant A/G snv 0.68
CUI: C0455806
Disease: Infant length
Infant length
0.700 1.000 1 2015 2015
dbSNP: rs28584580
rs28584580
15 88854596 intron variant A/G snv 0.11
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs28584580
rs28584580
15 88854596 intron variant A/G snv 0.11
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution
0.700 1.000 1 2019 2019
dbSNP: rs72765671
rs72765671
15 88817911 intron variant A/G snv 0.10
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs4932200
rs4932200
15 88806477 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1516794
rs1516794
1.000 0.040 15 88861672 intron variant A/T snv 5.3E-03
CUI: C0271183
Disease: Severe myopia
Severe myopia
0.020 1.000 2 2011 2014
dbSNP: rs3817428
rs3817428
15 88872016 missense variant C/G snv 0.20 0.20
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution
0.700 1.000 1 2019 2019
dbSNP: rs3817428
rs3817428
15 88872016 missense variant C/G snv 0.20 0.20
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs3817428
rs3817428
15 88872016 missense variant C/G snv 0.20 0.20
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2015 2015
dbSNP: rs16942341
rs16942341
15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2010 2019
dbSNP: rs16942341
rs16942341
15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02
CUI: C0489786
Disease: Height
Height
0.700 1.000 2 2010 2011
dbSNP: rs16942341
rs16942341
15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02
CUI: C0424678
Disease: Lean body mass
Lean body mass
0.700 1.000 1 2019 2019
dbSNP: rs2351491
rs2351491
15 88854874 synonymous variant C/T snv 0.50 0.48
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2011 2011
dbSNP: rs2351491
rs2351491
15 88854874 synonymous variant C/T snv 0.50 0.48
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2011 2011
dbSNP: rs3784757
rs3784757
1.000 0.040 15 88860173 intron variant G/A snv 0.13
CUI: C0271183
Disease: Severe myopia
Severe myopia
0.020 1.000 2 2011 2014
dbSNP: rs121913568
rs121913568
1.000 0.080 15 88872038 missense variant G/A snv
Spondyloepimetaphyseal Dysplasia, Aggrecan Type
0.800 1.000 1 2009 2009
dbSNP: rs56071466
rs56071466
15 88827235 intron variant G/A snv 0.50
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019