ADAM23, ADAM metallopeptidase domain 23, 8745

N. diseases: 49; N. variants: 12
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: rs1448903
rs1448903
2 206444237 intron variant A/G snv 6.1E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 3 2018 2019
dbSNP: rs10490744
rs10490744
1.000 0.040 2 206596559 intron variant G/A snv 7.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10490745
rs10490745
1.000 0.040 2 206601836 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13429599
rs13429599
2 206548901 intron variant G/A snv 0.25
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2019 2019
dbSNP: rs143219430
rs143219430
2 206527534 intron variant A/C snv 1.3E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs1921673
rs1921673
2 206459558 intron variant A/G snv 0.70
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs1991537
rs1991537
1.000 0.040 2 206607849 intron variant A/G snv 0.40
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2359677
rs2359677
1.000 0.040 2 206597918 intron variant G/T snv 6.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs33998651
rs33998651
2 206517977 intron variant G/A snv 1.8E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs3755226
rs3755226
1.000 0.040 2 206613925 intron variant T/C snv 6.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs3821172
rs3821172
1.000 0.040 2 206600240 intron variant C/G snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6435342
rs6435342
1.000 0.040 2 206601106 intron variant A/G snv 0.49
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017