Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146113475
rs146113475
Entrez Id: 27242
Gene Symbol: TNFRSF21
TNFRSF21
CUI: C0271183
Disease:
Severe myopia 		0.010 GeneticVariation BEFREE WES identified a novel TNF receptor superfamily member 21 (<i>TNFRSF21</i>) variant, P146A, in a large Chinese family with HM, and another three rare heterozygous variants (P202L, E240* and A440G) in <i>TNFRSF21</i> were found in 220 unrelated cases with HM. 31189563 2019
dbSNP: rs779058448
rs779058448
Entrez Id: 27242
Gene Symbol: TNFRSF21
TNFRSF21
CUI: C0271183
Disease:
Severe myopia 		0.010 GeneticVariation BEFREE WES identified a novel TNF receptor superfamily member 21 (<i>TNFRSF21</i>) variant, P146A, in a large Chinese family with HM, and another three rare heterozygous variants (P202L, E240* and A440G) in <i>TNFRSF21</i> were found in 220 unrelated cases with HM. 31189563 2019