List of variants in gene IL36RN reported as uncertain significance by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_012275.3(IL36RN):c.*276A>G	rs1800930	0.64674
NM_012275.3(IL36RN):c.*418A>G	rs3180235	0.64649
NM_012275.3(IL36RN):c.*560C>G	rs2472188	0.64649
NM_012275.3(IL36RN):c.*222T>C	rs2515401	0.64643
NM_012275.3(IL36RN):c.*326C>A	rs2515402	0.64633
NM_012275.3(IL36RN):c.*401A>T	rs3180234

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