Source: CURATED

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: rs11762085
rs11762085
AHCYL2
1.000 0.040 7 129390821 intron variant G/A snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11766298
rs11766298
AHCYL2
7 129365006 intron variant C/T snv 3.5E-02
CUI: C3547188
Disease: response to fenofibrate
response to fenofibrate 		0.700 1.000 1 2012 2012
dbSNP: rs12540568
rs12540568
AHCYL2
1.000 0.040 7 129400669 intron variant A/G snv 0.28
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs12667132
rs12667132
AHCYL2
1.000 0.040 7 129380179 intron variant G/C snv 0.31
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13246455
rs13246455
AHCYL2
1.000 0.040 7 129381072 intron variant T/C snv 2.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1559486
rs1559486
AHCYL2 ; LOC107986847
1.000 0.040 7 129376053 intron variant C/T snv 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17552411
rs17552411
AHCYL2
1.000 0.040 7 129400177 intron variant T/C snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17552570
rs17552570
AHCYL2
1.000 0.040 7 129407527 intron variant A/G snv 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs180825777
rs180825777
AHCYL2 ; LOC107986847
7 129370682 intron variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6467244
rs6467244
AHCYL2
1.000 0.040 7 129409666 intron variant A/G snv 0.84
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6953598
rs6953598
AHCYL2
1.000 0.040 7 129393900 intron variant G/A snv 0.28
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs822040
rs822040
AHCYL2
1.000 0.040 7 129426081 intron variant G/C snv 0.32
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs9641850
rs9641850
AHCYL2
1.000 0.040 7 129393042 intron variant G/T snv 0.28
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017