LARP4B, La ribonucleoprotein 4B, 23185

N. diseases: 22; N. variants: 7
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: rs80282103
rs80282103 		1.000 0.080 10 853131 intron variant A/T snv 0.12
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 5 2017 2019
dbSNP: rs11253511
rs11253511 		10 918892 intron variant C/T snv 0.16
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs112889159
rs112889159 		10 853363 intron variant A/T snv 6.9E-03
CUI: C4268744
Disease: Atypical femoral fracture
Atypical femoral fracture 		0.700 1.000 1 2019 2019
dbSNP: rs12264390
rs12264390 		10 913171 intron variant T/C snv 0.20
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs12264390
rs12264390 		10 913171 intron variant T/C snv 0.20
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12762973
rs12762973 		10 914821 intron variant C/A;G snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs141536087
rs141536087 		1.000 0.080 10 808752 intron variant ACACACACACACACAC/-;ACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC delins
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7908590
rs7908590 		10 906583 intron variant C/G snv 4.7E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs80282103
rs80282103 		1.000 0.080 10 853131 intron variant A/T snv 0.12
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs80282103
rs80282103 		1.000 0.080 10 853131 intron variant A/T snv 0.12
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs80282103
rs80282103 		1.000 0.080 10 853131 intron variant A/T snv 0.12
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2017 2017