List of variants in gene TMEM126A reported as likely benign for optic atrophy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_032273.4(TMEM126A):c.314G>A (p.Arg105Gln)	rs146573578	0.00247
NM_032273.4(TMEM126A):c.562T>A (p.Ser188Thr)	rs34397695	0.00240
NM_032273.4(TMEM126A):c.154A>G (p.Ser52Gly)	rs140047528	0.00239
NM_032273.4(TMEM126A):c.96T>G (p.Leu32=)	rs36100288	0.00220
NM_032273.4(TMEM126A):c.191G>A (p.Arg64His)	rs11556797	0.00161
NM_032273.4(TMEM126A):c.280+14C>T	rs117453673	0.00039

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