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: rs6430538
rs6430538
CCNT2-AS1
0.925 0.080 2 134782397 intron variant C/T snv 0.62
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.830 1.000 3 2012 2019
dbSNP: rs6710823
rs6710823
CCNT2-AS1
1.000 0.040 2 134834811 intron variant G/A snv 0.23
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.800 1.000 1 2011 2012
dbSNP: rs10198552
rs10198552
ACMSD ; CCNT2-AS1
2 134842306 intron variant T/C snv 6.2E-02
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12473839
rs12473839
ACMSD ; CCNT2-AS1
2 134880474 intron variant C/T snv 0.50
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4954174
rs4954174
CCNT2-AS1
2 134774133 intron variant A/G snv 0.32
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4954192
rs4954192
ACMSD ; CCNT2-AS1
1.000 0.080 2 134875411 intron variant C/T snv 0.52
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs4954192
rs4954192
ACMSD ; CCNT2-AS1
1.000 0.080 2 134875411 intron variant C/T snv 0.52
CUI: C0202231
Disease: Thyroxine measurement
Thyroxine measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4954192
rs4954192
ACMSD ; CCNT2-AS1
1.000 0.080 2 134875411 intron variant C/T snv 0.52
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2015 2015
dbSNP: rs62168891
rs62168891
CCNT2-AS1
2 134914617 intron variant C/T snv 0.58
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs62168891
rs62168891
CCNT2-AS1
2 134914617 intron variant C/T snv 0.58
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs6430549
rs6430549
ACMSD ; CCNT2-AS1
2 134858776 intron variant A/G snv 0.58
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2017 2017
dbSNP: rs6727396
rs6727396
CCNT2-AS1
2 134741666 intron variant A/C snv 0.27
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019