SPATA13, spermatogenesis associated 13, 221178

N. diseases: 15; N. variants: 5
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: rs715921
rs715921 		13 24221351 intron variant G/A snv 0.28
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.800 1.000 1 2012 2012
dbSNP: rs7329958
rs7329958 		13 24207942 intron variant T/A;C snv
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9507287
rs9507287 		0.851 0.040 13 24212439 intron variant T/C snv 0.24
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs9507287
rs9507287 		0.851 0.040 13 24212439 intron variant T/C snv 0.24
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs9507287
rs9507287 		0.851 0.040 13 24212439 intron variant T/C snv 0.24
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs9507287
rs9507287 		0.851 0.040 13 24212439 intron variant T/C snv 0.24
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9507287
rs9507287 		0.851 0.040 13 24212439 intron variant T/C snv 0.24
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9511143
rs9511143 		1.000 0.040 13 24200509 intron variant C/T snv 0.56
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1220597
rs1220597 		0.925 13 24243875 intron variant C/T snv 0.51
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
Differentiated Thyroid Gland Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs1220597
rs1220597 		0.925 13 24243875 intron variant C/T snv 0.51
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
Primary differentiated carcinoma of thyroid gland 		0.010 1.000 1 2014 2014