List of variants in gene combination GPHN, RDH12 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_152443.3(RDH12):c.317G>A (p.Arg106Gln)	rs150812168	0.00017
NM_152443.3(RDH12):c.-123C>T	rs960563752	0.00009
NM_152443.3(RDH12):c.343+5G>A	rs1236938342	0.00001
NM_152443.3(RDH12):c.100A>C (p.Asn34His)	rs2503792596
NM_152443.3(RDH12):c.72G>C (p.Lys24Asn)	rs2503792333

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