List of variants in gene combination LOC124629354, PRPH, TROAP reported as not provided by Epithelial Biology; Institute of Medical Biology, Singapore

Minimum submission review status:		Collection method:
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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006262.4(PRPH):c.1107A>G (p.Lys369=)	rs73112143	0.24810
NM_006262.4(PRPH):c.1217+43C>A	rs112146976	0.05942
NM_006262.4(PRPH):c.1083C>G (p.Leu361=)	rs62636517	0.01563
NM_006262.4(PRPH):c.1217+27C>A	rs200141011	0.01155
NM_006262.4(PRPH):c.870+12G>A	rs267607531	0.00002
NM_006262.4(PRPH):c.1108G>A (p.Glu370Lys)	rs59827092	0.00001
NM_006262.4(PRPH):c.1217+34G>A	rs267607532

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