List of variants in gene SAMHD1 reported as likely benign for autoimmune disease

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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_015474.4(SAMHD1):c.334G>A (p.Val112Ile)	rs144353824	0.00029
NM_015474.4(SAMHD1):c.1393C>A (p.Gln465Lys)	rs142393072	0.00012
NM_015474.4(SAMHD1):c.697-11A>G	rs200458478	0.00011
NM_015474.4(SAMHD1):c.993C>T (p.Tyr331=)	rs775726168	0.00004
NM_015474.4(SAMHD1):c.144G>A (p.Glu48=)	rs140157384	0.00001
NM_015474.4(SAMHD1):c.401G>A (p.Arg134Gln)	rs767413799	0.00001

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