Source: GWASCAT

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: rs1727313
rs1727313
MPHOSPH9
1.000 0.080 12 123156306 3 prime UTR variant C/G snv 0.84
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 1 2014 2014
dbSNP: rs1790100
rs1790100
MPHOSPH9
1.000 0.080 12 123172178 intron variant G/T snv 0.63
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2009 2009
dbSNP: rs1615350
rs1615350
MPHOSPH9
1.000 0.040 12 123165788 intron variant C/T snv 0.58
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 3 2017 2019
dbSNP: rs2851447
rs2851447
MPHOSPH9
1.000 0.040 12 123180566 intron variant G/C snv 0.59
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 3 2014 2018
dbSNP: rs10654220
rs10654220
MPHOSPH9
1.000 0.040 12 123218875 intron variant -/TGT;TGTTGT delins
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.700 1.000 1 2019 2019
dbSNP: rs10654220
rs10654220
MPHOSPH9
1.000 0.040 12 123218875 intron variant -/TGT;TGTTGT delins
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1615350
rs1615350
MPHOSPH9
1.000 0.040 12 123165788 intron variant C/T snv 0.58
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs1716162
rs1716162
MPHOSPH9
12 123157991 intron variant T/A snv 0.63
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs1790105
rs1790105
MPHOSPH9
12 123183403 intron variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2102949
rs2102949
MPHOSPH9
1.000 0.040 12 123192216 intron variant G/A snv 0.59
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs2695478
rs2695478
MPHOSPH9
12 123204974 intron variant C/T snv 0.84
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2851436
rs2851436
MPHOSPH9
12 123182807 intron variant G/T snv 0.64
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2019 2019
dbSNP: rs2851437
rs2851437
MPHOSPH9
12 123169045 intron variant C/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs2851447
rs2851447
MPHOSPH9
1.000 0.040 12 123180566 intron variant G/C snv 0.59
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs61041384
rs61041384
MPHOSPH9
1.000 0.040 12 123159496 intron variant T/C snv 4.5E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017