Source: GWASCAT

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: rs10002854
rs10002854
SORCS2
1.000 0.040 4 7519419 intron variant C/T snv 8.8E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10023470
rs10023470
SORCS2 ; PSAPL1
4 7432729 3 prime UTR variant A/G snv 0.20
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10470722
rs10470722
SORCS2
1.000 0.040 4 7516784 intron variant C/T snv 8.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10937844
rs10937844
SORCS2
1.000 0.040 4 7624252 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs111913416
rs111913416
SORCS2
4 7706148 intron variant A/T snv 0.19
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs11731003
rs11731003
SORCS2
1.000 0.080 4 7388545 intron variant C/G;T snv
CUI: C0236663
Disease: Alcohol withdrawal syndrome
Alcohol withdrawal syndrome 		0.700 1.000 1 2018 2018
dbSNP: rs12642344
rs12642344
SORCS2
1.000 0.040 4 7623904 intron variant C/T snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13114336
rs13114336
SORCS2
1.000 0.040 4 7517591 intron variant G/C snv 5.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13125782
rs13125782
SORCS2
1.000 0.040 4 7426539 intron variant T/A;C;G snv
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		0.700 1.000 1 2017 2017
dbSNP: rs35791045
rs35791045
SORCS2
4 7425380 intron variant A/G snv 0.11
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4234795
rs4234795
SORCS2
1.000 0.080 4 7209075 intron variant A/C;G;T snv
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.700 1.000 1 2017 2017
dbSNP: rs4689642
rs4689642
SORCS2
1.000 0.040 4 7213595 intron variant A/G;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.700 1.000 1 2015 2015
dbSNP: rs4689803
rs4689803
SORCS2
1.000 0.040 4 7623930 intron variant T/A snv 0.77
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6446592
rs6446592
SORCS2
0.925 0.040 4 7340998 intron variant T/C snv 0.17
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs6446592
rs6446592
SORCS2
0.925 0.040 4 7340998 intron variant T/C snv 0.17
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs6838261
rs6838261
SORCS2
1.000 0.040 4 7623685 intron variant T/C snv 0.31
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs73214671
rs73214671
SORCS2
4 7570384 intron variant G/A snv 1.5E-02
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		0.700 1.000 1 2017 2017
dbSNP: rs744355
rs744355
SORCS2
1.000 0.040 4 7521637 intron variant T/C snv 0.35
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs744356
rs744356
SORCS2
1.000 0.040 4 7521546 intron variant C/T snv 0.72
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs77191210
rs77191210
SORCS2 ; PSAPL1
4 7434974 intron variant C/T snv 0.16
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018