List of variants in gene PDE6B studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_000283.4(PDE6B):c.958G>A (p.Val320Ile)	rs10902758	0.99926
NM_000283.4(PDE6B):c.*12A>G	rs28675771	0.58217
NM_000283.4(PDE6B):c.915G>A (p.Thr305=)	rs75695239	0.05186
NM_000283.4(PDE6B):c.1467+20C>T	rs74464382	0.05011
NM_000283.4(PDE6B):c.143G>A (p.Arg48Gln)	rs113842820	0.02573
NM_000283.4(PDE6B):c.123G>A (p.Pro41=)	rs113459274	0.02570
NM_000283.4(PDE6B):c.373C>G (p.Pro125Ala)	rs28414606	0.02568
NM_000283.4(PDE6B):c.384C>T (p.Ser128=)	rs28510278	0.02567
NM_000283.4(PDE6B):c.2289G>A (p.Lys763=)	rs61739716	0.01153
NM_000283.4(PDE6B):c.873T>C (p.Ser291=)	rs142597807	0.00827
NM_000283.4(PDE6B):c.615C>T (p.Asp205=)	rs149293844	0.00577
NM_000283.4(PDE6B):c.1467+18G>A	rs140243735	0.00555
NM_000283.4(PDE6B):c.655T>C (p.Tyr219His)	rs62295357	0.00465
NM_000283.4(PDE6B):c.270C>T (p.Asp90=)	rs80344633	0.00422
NM_000283.4(PDE6B):c.711+10C>T	rs201100689	0.00237
NM_000283.4(PDE6B):c.145G>T (p.Asp49Tyr)	rs79826315	0.00091
NM_000283.4(PDE6B):c.1497T>G (p.Phe499Leu)	rs150000610	0.00078
NM_000283.4(PDE6B):c.1401+4C>T	rs113246945	0.00077
NM_000283.4(PDE6B):c.1401+7_1401+8insA	rs537010934	0.00074
NM_000283.4(PDE6B):c.905G>A (p.Gly302Asp)	rs146646008	0.00041
NM_000283.4(PDE6B):c.2129+8C>T	rs764138476	0.00004
NM_000283.4(PDE6B):c.132C>G (p.Cys44Trp)	rs199974771	0.00003
NM_000283.4(PDE6B):c.1920+2T>C	rs763996159	0.00001
NM_000283.4(PDE6B):c.928-9_940dup	rs539992414

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