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: rs111906841
rs111906841
PXYLP1
3 141242812 intron variant A/G snv 1.5E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1346408
rs1346408
PXYLP1 ; ZBTB38
3 141353447 intron variant C/T snv 0.55
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1346408
rs1346408
PXYLP1 ; ZBTB38
3 141353447 intron variant C/T snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1567558
rs1567558
PXYLP1
3 141289281 intron variant A/G snv 0.50
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs1567558
rs1567558
PXYLP1
3 141289281 intron variant A/G snv 0.50
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs28721484
rs28721484
PXYLP1 ; ZBTB38
3 141334437 intron variant C/T snv 0.22
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs28721484
rs28721484
PXYLP1 ; ZBTB38
3 141334437 intron variant C/T snv 0.22
CUI: C0005910
Disease: Body Weight
Body Weight 		0.700 1.000 1 2017 2017
dbSNP: rs34655123
rs34655123
PXYLP1 ; ZBTB38
3 141348246 intron variant A/G snv 4.7E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs55768579
rs55768579
PXYLP1 ; ZBTB38
3 141340945 intron variant GA/- delins 1.3E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs6440001
rs6440001
PXYLP1 ; ZBTB38
3 141367130 3 prime UTR variant T/C snv 0.52
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs6784404
rs6784404
PXYLP1 ; ZBTB38
3 141354833 intron variant G/A snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs726838
rs726838
PXYLP1 ; ZBTB38
3 141353824 intron variant A/T snv 0.27
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs7613516
rs7613516
PXYLP1 ; ZBTB38
3 141360467 intron variant T/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs9866391
rs9866391
PXYLP1 ; ZBTB38
1.000 0.040 3 141357242 intron variant T/C snv 0.41
CUI: C0027092
Disease: Myopia
Myopia 		0.700 1.000 1 2016 2016
dbSNP: rs9866391
rs9866391
PXYLP1 ; ZBTB38
1.000 0.040 3 141357242 intron variant T/C snv 0.41
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013