rs498872, PHLDB1

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Glioma
CUI: C0017638
Disease: Glioma
353 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.900 0.941 17 2009 2020
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
72 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.700 1.000 2 2009 2011
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.700 1.000 1 2010 2010
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.040 0.750 4 2010 2017
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.030 1.000 3 2011 2020
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.020 1.000 2 2011 2015
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.010 1.000 1 2011 2011
Asthma
CUI: C0004096
Disease: Asthma
1536 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.010 1.000 1 2010 2010
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.010 1.000 1 2011 2011
Chromosome 10, monosomy 10q
CUI: C0795839
Disease: Chromosome 10, monosomy 10q
4 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 0.010 1.000 1 2013 2013