List of variants in gene PCDH15 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001384140.1(PCDH15):c.1138G>A (p.Gly380Ser)	rs10825269	0.22813
NM_001384140.1(PCDH15):c.4024C>A (p.Gln1342Lys)	rs61731387	0.00699
NM_033056.4(PCDH15):c.4850A>G (p.Asn1617Ser)	rs111033362	0.00631
NM_001384140.1(PCDH15):c.3983+12T>C	rs149867749	0.00483
NM_001384140.1(PCDH15):c.4672-1640A>G	rs145178582	0.00232
NM_033056.4(PCDH15):c.4812G>T (p.Arg1604Ser)	rs148718874	0.00066
NM_001384140.1(PCDH15):c.3451G>A (p.Gly1151Arg)	rs149478475	0.00039
NM_001384140.1(PCDH15):c.3502-6G>A	rs749897896	0.00028
NM_001384140.1(PCDH15):c.4308GCC[7] (p.Pro1442_Pro1443dup)	rs559130985
NM_001384140.1(PCDH15):c.4672-1444_4672-1441dup	rs373720521
NM_033056.4(PCDH15):c.5294_5302del (p.Leu1765_Pro1767del)	rs557936064

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