RASA2, RAS p21 protein activator 2, 5922

N. diseases: 116; N. variants: 18
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: rs16851483
rs16851483
0.925 0.080 3 141556594 intron variant G/T snv 6.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2015 2019
dbSNP: rs9819371
rs9819371
3 141487958 intron variant C/T snv 4.7E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 2 2016 2019
dbSNP: rs10663129
rs10663129
3 141602994 intron variant -/CT delins 0.29
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs115380769
rs115380769
3 141614997 3 prime UTR variant C/T snv 4.8E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs116542483
rs116542483
3 141605663 intron variant C/A;G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs11714208
rs11714208
3 141576208 intron variant A/G snv 0.28
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11917587
rs11917587
3 141488733 intron variant G/A snv 0.55
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs16851483
rs16851483
0.925 0.080 3 141556594 intron variant G/T snv 6.7E-02
CUI: C0037369
Disease: Smoking
Smoking
Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs2035935
rs2035935
3 141587171 intron variant A/G;T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs2035935
rs2035935
3 141587171 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs295322
rs295322
3 141607760 splice region variant T/C snv 0.12 0.13
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs36013391
rs36013391
3 141497704 intron variant AAAAAA/-;AAAA;AAAAA;AAAAAAA delins
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs3732869
rs3732869
3 141576936 intron variant T/A snv 0.13
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs3732869
rs3732869
3 141576936 intron variant T/A snv 0.13
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs3821709
rs3821709
3 141561431 intron variant T/C snv 6.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs6776003
rs6776003
1.000 0.080 3 141547651 intron variant G/A snv 0.55
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6776003
rs6776003
1.000 0.080 3 141547651 intron variant G/A snv 0.55
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2012 2012
dbSNP: rs6776003
rs6776003
1.000 0.080 3 141547651 intron variant G/A snv 0.55
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs6808837
rs6808837
3 141499112 intron variant T/C snv 0.43
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs7651511
rs7651511
3 141513090 intron variant G/A snv 0.29
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs78074823
rs78074823
3 141571742 intron variant C/A snv 1.3E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs79308158
rs79308158
3 141529673 intron variant A/C;G snv 4.8E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs79308158
rs79308158
3 141529673 intron variant A/C;G snv 4.8E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs9289634
rs9289634
3 141532813 intron variant A/C;G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9819371
rs9819371
3 141487958 intron variant C/T snv 4.7E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016