DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: FPGT-TNNI3K ×

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs201167096	FPGT-TNNI3K ; LRRC53 ; TNNI3K			1	74534327	intron variant	-/T	delins			2
rs113313252	TNNI3K ; FPGT-TNNI3K ; LRRC53			1	74534327	intron variant	-/T	delins			2
rs1514175	TNNI3K ; LRRC53 ; FPGT-TNNI3K	1.000	0.080	1	74525960	intron variant	A/G	snv		0.48	2
rs12142020	TNNI3K ; LRRC53 ; FPGT-TNNI3K			1	74534327	intron variant	A/T	snv		0.50	2
rs1514174	LRRC53 ; FPGT-TNNI3K ; TNNI3K	1.000	0.080	1	74527379	intron variant	C/T	snv		0.44	1
rs1040070	LRRC53 ; FPGT-TNNI3K ; TNNI3K	1.000	0.080	1	74512186	intron variant	G/A;C	snv			1
rs1514177	TNNI3K ; FPGT-TNNI3K ; LRRC53	1.000	0.080	1	74525718	intron variant	C/G	snv		0.49	1