List of variants in gene AIPL1 reported as likely benign for Retinitis Pigmentosa, Recessive

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_014336.5(AIPL1):c.*606G>A	rs10852881	0.63496
NM_014336.5(AIPL1):c.300A>G (p.Leu100=)	rs8075035	0.60839
NM_014336.5(AIPL1):c.277-10A>C	rs12453262	0.52383
NM_014336.5(AIPL1):c.*753G>A	rs62060993	0.51826
NM_014336.5(AIPL1):c.*1391C>T	rs907939	0.11244
NM_014336.5(AIPL1):c.*1202C>T	rs907937	0.10352
NM_014336.4(AIPL1):c.-106C>A	rs7211442	0.10081
NM_014336.5(AIPL1):c.*1018G>A	rs2871287	0.08814
NM_014336.5(AIPL1):c.*1658T>C	rs78526307	0.05230
NM_014336.5(AIPL1):c.111C>T (p.Phe37=)	rs11650007	0.02008
NM_014336.5(AIPL1):c.341C>T (p.Thr114Ile)	rs8069375	0.01781
NM_014336.5(AIPL1):c.*134G>T	rs2090068	0.01001
NM_014336.5(AIPL1):c.*1178C>T	rs149460055	0.00841
NM_014336.5(AIPL1):c.*1237C>T	rs139074266	0.00803
NM_014336.5(AIPL1):c.*188G>A	rs1317185	0.00763
NM_014336.5(AIPL1):c.642+14G>A	rs188779461	0.00682
NM_014336.5(AIPL1):c.765T>C (p.Asp255=)	rs62637018	0.00643
NM_014336.5(AIPL1):c.277-14G>A	rs117749485	0.00585
NM_014336.5(AIPL1):c.97-9G>A	rs140124986	0.00457
NM_014336.5(AIPL1):c.*390G>T	rs182504714	0.00334
NM_014336.5(AIPL1):c.*221G>A	rs112307858	0.00302
NM_014336.5(AIPL1):c.516T>C (p.His172=)	rs62637017	0.00220
NM_014336.5(AIPL1):c.*33A>C	rs140472462	0.00126
NM_014336.4(AIPL1):c.-107C>G	rs149098937	0.00093
NM_014336.5(AIPL1):c.*824G>C	rs145706166	0.00065
NM_014336.5(AIPL1):c.*1289G>A	rs11869118
NM_014336.5(AIPL1):c.151_152del	rs77115868
NM_014336.5(AIPL1):c.*1568G>A	rs11869066

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