NCK1, NCK adaptor protein 1, 4690

N. diseases: 51; N. variants: 4
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: rs11715604
rs11715604
0.851 0.160 3 136870707 intron variant A/G;T snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs11715604
rs11715604
0.851 0.160 3 136870707 intron variant A/G;T snv
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs11715604
rs11715604
0.851 0.160 3 136870707 intron variant A/G;T snv
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs11715604
rs11715604
0.851 0.160 3 136870707 intron variant A/G;T snv
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs6800032
rs6800032
3 136903718 intron variant C/T snv 0.68
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs9867325
rs9867325
3 136900067 non coding transcript exon variant G/C snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2015 2015
dbSNP: rs9879531
rs9879531
3 136920133 intron variant A/G snv 0.17
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2019 2019