SNTG2, syntrophin gamma 2, 54221

N. diseases: 2; N. variants: 2
Source: CURATED ×
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: rs13382275
rs13382275 		1.000 0.040 2 969893 intron variant A/G snv 0.12
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs13382275
rs13382275 		1.000 0.040 2 969893 intron variant A/G snv 0.12
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2015 2015
dbSNP: rs6759670
rs6759670 		2 954605 intron variant C/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019