FPGT-TNNI3K, FPGT-TNNI3K readthrough, 100526835

N. diseases: 12; N. variants: 23
Disease: Body mass index procedure ×
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: rs1514175
rs1514175 		1.000 0.080 1 74525960 intron variant A/G snv 0.48
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 3 2010 2013
dbSNP: rs113313252
rs113313252 		1 74534327 intron variant -/T delins
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013
dbSNP: rs12142020
rs12142020 		1 74534327 intron variant A/T snv 0.50
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013
dbSNP: rs201167096
rs201167096 		1 74534327 intron variant -/T delins
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013