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: rs2056417
rs2056417
PEX14
1 10521601 intron variant G/A snv 0.25
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.800 1.000 1 2013 2013
dbSNP: rs616488
rs616488
PEX14
0.925 0.080 1 10506158 intron variant A/G snv 0.27
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.710 1.000 4 2013 2017
dbSNP: rs636291
rs636291
PEX14
0.925 0.080 1 10496040 intron variant G/A snv 0.55
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.710 1.000 2 2014 2018
dbSNP: rs10864459
rs10864459
PEX14
1.000 0.080 1 10503552 intron variant A/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs10864462
rs10864462
PEX14
1 10552101 intron variant A/T snv 0.11
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs12045923
rs12045923
PEX14
1 10583772 intron variant C/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2019 2019
dbSNP: rs142020459
rs142020459
PEX14
1.000 0.080 1 10512026 intron variant C/G snv 1.8E-02
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs17035390
rs17035390
PEX14
1.000 0.080 1 10593565 intron variant T/C snv 3.6E-02
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs2242288
rs2242288
PEX14
1.000 0.080 1 10624041 intron variant C/A snv 4.6E-02
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs2506889
rs2506889
PEX14
1.000 0.080 1 10535965 non coding transcript exon variant C/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs616402
rs616402
PEX14
1 10506215 intron variant C/T snv 0.29
CUI: C0425782
Disease: Breast size
Breast size 		0.700 1.000 1 2016 2016
dbSNP: rs648324
rs648324
PEX14
1 10496390 intron variant G/C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs648324
rs648324
PEX14
1 10496390 intron variant G/C;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs662064
rs662064
PEX14
1.000 0.080 1 10497194 intron variant T/C snv 0.66
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2016 2016
dbSNP: rs6687430
rs6687430
PEX14
1 10573188 intron variant G/A snv 0.48
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs6687430
rs6687430
PEX14
1 10573188 intron variant G/A snv 0.48
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019