SEPTIN4-AS1, SEPTIN4 antisense RNA 1, 101927688

N. diseases: 3; 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: rs9905704
rs9905704 		1.000 0.120 17 58555182 intron variant G/T snv 0.77
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		Neoplasms; Male Urogenital Diseases; Endocrine System Diseases 0.810 1.000 4 2013 2017
dbSNP: rs9905704
rs9905704 		1.000 0.120 17 58555182 intron variant G/T snv 0.77
CUI: C0039590
Disease: Testicular Neoplasms
Testicular Neoplasms 		Neoplasms; Male Urogenital Diseases; Endocrine System Diseases 0.700 1.000 2 2013 2013
dbSNP: rs113162402
rs113162402 		17 58522103 splice acceptor variant T/A snv
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs740605
rs740605 		17 58527450 non coding transcript exon variant C/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs375038332
rs375038332 		1.000 0.040 17 58521810 missense variant G/A snv
CUI: C1834304
Disease: AMYOTROPHY, HEREDITARY NEURALGIC
AMYOTROPHY, HEREDITARY NEURALGIC 		Nervous System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs758377
rs758377 		0.925 0.080 17 58529763 intron variant T/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2009 2009
dbSNP: rs758377
rs758377 		0.925 0.080 17 58529763 intron variant T/C;G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2009 2009