Disease: Body Height ×
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: rs2573652
rs2573652 		15 99974409 missense variant T/C;G snv 0.66; 4.0E-06
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2015 2019
dbSNP: rs72755233
rs72755233 		1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2017 2019
dbSNP: rs145482150
rs145482150 		15 99993107 missense variant C/T snv 2.0E-04 2.0E-04
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs149578709
rs149578709 		15 100132203 intron variant A/G snv 9.0E-03 5.2E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2573625
rs2573625 		15 99972953 3 prime UTR variant C/T snv 0.62
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2014 2014
dbSNP: rs2581348
rs2581348 		15 99973858 3 prime UTR variant C/T snv 0.63
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2727195
rs2727195 		15 99972912 3 prime UTR variant G/A snv 0.61
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs28411867
rs28411867 		15 100314288 intron variant C/T snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs397807524
rs397807524 		15 100052239 intron variant -/AA ins 7.0E-06
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4369638
rs4369638 		15 100254158 synonymous variant C/T snv 0.75 0.76
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4467054
rs4467054 		15 100255167 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4533267
rs4533267 		15 100246066 intron variant A/G snv 0.63
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2008 2008
dbSNP: rs4965593
rs4965593 		15 100218180 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs4965598
rs4965598 		15 100219409 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs4965612
rs4965612 		15 100261237 intron variant A/G snv 0.72
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs76301628
rs76301628 		15 100183232 intron variant G/T snv 3.4E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019