SPATA13, spermatogenesis associated 13, 221178

N. diseases: 15; N. variants: 5
Disease: Hypothyroidism ×
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: 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: 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