BOLL, boule homolog, RNA binding protein, 66037

N. diseases: 15; N. variants: 18
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: rs700651
rs700651
1.000 0.080 2 197766990 intron variant G/A snv 0.73
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
Nervous System Diseases; Cardiovascular Diseases 0.820 1.000 3 2008 2019
dbSNP: rs1851779
rs1851779
1.000 0.080 2 197782384 intron variant C/T snv 0.19
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2293255
rs2293255
1.000 0.080 2 197756782 intron variant T/C snv 0.20
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2012 2012
dbSNP: rs700641
rs700641
2 197734509 intron variant C/A;T snv
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms
0.700 1.000 1 2016 2016
dbSNP: rs700642
rs700642
2 197736006 intron variant T/G snv 0.73
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700643
rs700643
2 197736646 intron variant A/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700645
rs700645
2 197740790 intron variant A/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700646
rs700646
2 197743787 intron variant C/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700648
rs700648
2 197757912 intron variant C/T snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs700648
rs700648
2 197757912 intron variant C/T snv 0.50
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700649
rs700649
2 197758028 intron variant G/A snv 0.50
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700650
rs700650
2 197759561 intron variant G/A snv 0.50
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700653
rs700653
2 197772709 intron variant A/G snv 0.50
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700654
rs700654
2 197778697 intron variant G/A snv 0.50
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs700655
rs700655
2 197778907 intron variant G/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs700655
rs700655
2 197778907 intron variant G/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs770666
rs770666
2 197747173 intron variant T/A snv 0.50
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs771013
rs771013
2 197760513 intron variant G/A snv 0.50
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs140027779
rs140027779
2 197756444 missense variant T/C snv 8.0E-06 7.0E-06
CUI: C0021364
Disease: Male infertility
Male infertility
Male Urogenital Diseases 0.010 1.000 1 2004 2004
dbSNP: rs372015936
rs372015936
2 197743089 missense variant G/A;C snv 4.1E-05; 4.1E-06
CUI: C0021364
Disease: Male infertility
Male infertility
Male Urogenital Diseases 0.010 1.000 1 2004 2004
dbSNP: rs700651
rs700651
1.000 0.080 2 197766990 intron variant G/A snv 0.73
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2012 2012