List of variants in gene combination SAMHD1, TLDC2 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_015474.4(SAMHD1):c.*505T>A	rs747128919	0.00139
NM_015474.4(SAMHD1):c.*362G>A	rs886056646	0.00009
NM_015474.4(SAMHD1):c.*503A>G	rs757372495	0.00004
NM_015474.4(SAMHD1):c.*536C>T	rs886056645	0.00004
NM_015474.4(SAMHD1):c.*871G>A	rs1030352932	0.00002
NM_015474.4(SAMHD1):c.*104G>C	rs570535296	0.00001
NM_015474.4(SAMHD1):c.*648C>T	rs1414917474	0.00001
NM_015474.4(SAMHD1):c.1798G>A (p.Asp600Asn)	rs761596589	0.00001
NM_015474.4(SAMHD1):c.*711A>C	rs886056644
NM_015474.4(SAMHD1):c.*717G>C	rs1990092783
NM_015474.4(SAMHD1):c.*882T>C	rs1990087887

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