ClinVar (all) for Orgtrack (Select 505868) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 590976	NC_000023.11:g.12906538T>A	TLR8, TLR8-AS1	Single nucleotide variant	Osteoarthritis	Gassociation
Select item 590975	NC_000023.11:g.12906527G>C	TLR8, TLR8-AS1	Single nucleotide variant	Osteoarthritis	Gassociation
Select item 590889	NC_000001.11:g.17157671G>T	PADI4	Single nucleotide variant	Rheumatoid arthritis	Gassociation
Select item 590790	NM_012387.3(PADI4):c.341-15T>C	PADI4	Single nucleotide variant (intron variant)	Rheumatoid arthritis	Gassociation
Select item 587698	NM_004872.5(TMEM59):c.*23G>A	TMEM59	Single nucleotide variant (3 prime UTR variant)	Estrogen resistance syndrome	Grisk factor
Select item 587697	NM_000125.4(ESR1):c.*241T>A	ESR1	Single nucleotide variant (3 prime UTR variant +1 more)	Estrogen resistance syndrome	Grisk factor
Select item 252960	NM_000261.2(MYOC):c.823A>T (p.Lys275Ter)	MYOC (K275*)	Single nucleotide variant (nonsense)	Open-angle glaucoma	GUncertain significanceFDA Recognized database

ClinVar