List of variants in gene STING1 reported as likely benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_198282.4(STING1):c.762G>A (p.Ala254=)	rs11554777	0.00153
NM_198282.4(STING1):c.575G>T (p.Gly192Val)	rs201096097	0.00019
NM_198282.4(STING1):c.61G>A (p.Ala21Thr)	rs140011636	0.00016
NM_198282.4(STING1):c.992G>A (p.Arg331Gln)	rs370524913	0.00006
NM_198282.4(STING1):c.760-3T>C	rs759930084	0.00005
NM_198282.4(STING1):c.174G>T (p.Leu58=)	rs763523329	0.00001
NM_198282.4(STING1):c.175C>T (p.Leu59=)	rs760161824	0.00001

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