DNAH2, dynein axonemal heavy chain 2, 146754

N. diseases: 7; N. variants: 6
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16956936
rs16956936
1.000 0.120 17 7730374 intron variant C/A;T snv
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.800 1.000 1 2009 2009
dbSNP: rs12603355
rs12603355
17 7829719 intron variant C/T snv 0.32
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12945870
rs12945870
17 7834013 downstream gene variant C/G;T snv
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs12945870
rs12945870
17 7834013 downstream gene variant C/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs138420351
rs138420351
1.000 17 7796745 intron variant C/T snv 9.6E-03
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma
0.700 1.000 1 2018 2018
dbSNP: rs138420351
rs138420351
1.000 17 7796745 intron variant C/T snv 9.6E-03
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs138420351
rs138420351
1.000 17 7796745 intron variant C/T snv 9.6E-03
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs34121753
rs34121753
17 7830515 intron variant A/G snv 0.40 0.41
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs34121753
rs34121753
17 7830515 intron variant A/G snv 0.40 0.41
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs57985356
rs57985356
17 7831745 missense variant T/G snv 0.13 8.0E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019