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: rs10512248
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2008 2015
dbSNP: rs16909898
rs16909898
PTCH1 ; LOC100507346
9 95468726 intron variant A/G snv 8.4E-02 0.10
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 2 2010 2012
dbSNP: rs10512248
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.700 1.000 1 2017 2017
dbSNP: rs10512248
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.700 1.000 1 2017 2017
dbSNP: rs111532669
rs111532669
PTCH1
9 95446682 3 prime UTR variant C/T snv 1.8E-02
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2019 2019
dbSNP: rs111532669
rs111532669
PTCH1
9 95446682 3 prime UTR variant C/T snv 1.8E-02
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs113154802
rs113154802
PTCH1
9 95516131 intron variant C/T snv 7.9E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1355619
rs1355619
PTCH1
9 95507889 intron variant A/G snv 0.41
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs28446321
rs28446321
PTCH1
9 95504573 intron variant T/A snv 0.12
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs28457693
rs28457693
PTCH1
9 95455066 intron variant A/C;G;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs28510415
rs28510415
PTCH1
9 95482744 non coding transcript exon variant A/G snv 6.7E-02
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2016 2016
dbSNP: rs28620532
rs28620532
PTCH1
9 95454594 intron variant A/G snv 0.44
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs28701981
rs28701981
PTCH1
9 95455299 intron variant T/C snv 0.44
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4448343
rs4448343
PTCH1
9 95504088 intron variant A/C;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2014 2014
dbSNP: rs473902
rs473902
PTCH1
9 95493953 intron variant T/G snv 5.7E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs473902
rs473902
PTCH1
9 95493953 intron variant T/G snv 5.7E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs473902
rs473902
PTCH1
9 95493953 intron variant T/G snv 5.7E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs75614054
rs75614054
PTCH1
1.000 0.040 9 95513507 intron variant C/T snv 6.7E-02
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018
dbSNP: rs80155616
rs80155616
PTCH1
9 95481586 intron variant C/T snv 6.5E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019