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: rs7081208
rs7081208
FRMD4A
1.000 0.080 10 13949865 intron variant G/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2013 2013
dbSNP: rs10906522
rs10906522
FRMD4A
1.000 0.080 10 13865236 intron variant T/A;C snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs10906564
rs10906564
FRMD4A
1.000 0.040 10 14010027 intron variant A/G snv 0.40
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11258533
rs11258533
FRMD4A
10 13695768 intron variant C/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11258541
rs11258541
FRMD4A
10 13707228 non coding transcript exon variant G/A snv 0.32
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs11258541
rs11258541
FRMD4A
10 13707228 non coding transcript exon variant G/A snv 0.32
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs11258564
rs11258564
FRMD4A
10 13730905 intron variant A/C;G snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs11258564
rs11258564
FRMD4A
10 13730905 intron variant A/C;G snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2017 2017
dbSNP: rs11258793
rs11258793
FRMD4A
1.000 0.040 10 14009961 intron variant C/T snv 1.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11258795
rs11258795
FRMD4A
1.000 0.040 10 14014180 intron variant C/T snv 0.39
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11258796
rs11258796
FRMD4A
1.000 0.040 10 14014383 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs12413816
rs12413816
FRMD4A ; LOC105376426
10 13715765 intron variant G/T snv 0.31
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs12413816
rs12413816
FRMD4A ; LOC105376426
10 13715765 intron variant G/T snv 0.31
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs12570849
rs12570849
FRMD4A
1.000 0.040 10 14147601 intron variant T/C snv 1.7E-03
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome 		0.700 1.000 1 2017 2017
dbSNP: rs17153734
rs17153734
FRMD4A
0.925 0.040 10 13692801 non coding transcript exon variant C/G snv 2.5E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs17153734
rs17153734
FRMD4A
0.925 0.040 10 13692801 non coding transcript exon variant C/G snv 2.5E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs17314229
rs17314229
FRMD4A
1.000 0.080 10 13974159 intron variant C/T snv 4.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2013 2013
dbSNP: rs1887004
rs1887004
FRMD4A
0.882 0.040 10 13698917 intron variant T/C;G snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2019 2019
dbSNP: rs1887004
rs1887004
FRMD4A
0.882 0.040 10 13698917 intron variant T/C;G snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs1887004
rs1887004
FRMD4A
0.882 0.040 10 13698917 intron variant T/C;G snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2019 2019
dbSNP: rs2169323
rs2169323
FRMD4A ; LOC101928453
10 14081749 intron variant G/A snv 0.22
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2292367
rs2292367
FRMD4A
1.000 0.040 10 14008771 intron variant A/C snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2446581
rs2446581
FRMD4A
1.000 0.080 10 13966445 intron variant G/A snv 0.28
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2013 2013
dbSNP: rs2446588
rs2446588
FRMD4A
1.000 0.040 10 14011188 intron variant A/G snv 0.74
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2446597
rs2446597
FRMD4A
1.000 0.040 10 14007605 intron variant A/G snv 0.98
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017