List of variants in gene combination SAMHD1, TLDC2 reported as benign for autoimmune disease

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_015474.4(SAMHD1):c.*629C>T	rs8124728	0.05345
NM_015474.4(SAMHD1):c.*288A>G	rs114791229	0.00502
NM_080628.3(TLDC2):c.*28T>C	rs45595032	0.00466
NM_015474.4(SAMHD1):c.*1008C>G	rs116489517	0.00406
NM_015474.4(SAMHD1):c.*45C>T	rs115645414	0.00402
NM_015474.4(SAMHD1):c.*240G>A	rs143588093	0.00244
NM_015474.4(SAMHD1):c.*71C>A	rs138927042	0.00229
NM_015474.4(SAMHD1):c.*95T>C	rs147220022	0.00038
NM_015474.4(SAMHD1):c.*120C>T	rs188941712	0.00006

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