List of variants reported as risk factor for perceptual disorders

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000186.4(CFH):c.2237-543=	rs1410996	0.54454
NM_000186.4(CFH):c.184G>A (p.Val62Ile)	rs800292	0.40446
NM_000186.4(CFH):c.1204= (p.His402=)	rs1061170	0.36375
NM_001099667.3(ARMS2):c.205G>T (p.Ala69Ser)	rs10490924	0.22973
NM_002775.4(HTRA1):c.-625G>A	rs11200638	0.22958
NM_000186.4(CFH):c.3628C>T (p.Arg1210Cys)	rs121913059	0.00019
NM_000186.4(CFH):c.1507C>G (p.Pro503Ala)	rs570523689	0.00002
NM_178857.6(RP1L1):c.133C>T (p.Arg45Trp)	rs267607017	0.00001
CX3CR1:c.[841G>A;935C>T] (p.Val294Ile;Thr280Met)
NC_000010.11:g.122457305_122457748delinsTTATTAATTAATTAACTAAAATTAAATTATTTAGTTAATTTAATTAACTAAACT	rs2133900556
NM_000186.4(CFH):c.1419G>C (p.Ala473=)	rs2274700

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