List of variants in gene combination ATM, LOC130006700 reported as uncertain significance for immune system disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000051.3(ATM):c.-186G>A	rs879725890	0.00006
NM_000051.4(ATM):c.-94G>A	rs766115348	0.00006
NM_000051.3(ATM):c.-174A>C	rs928618464	0.00001
NM_000051.4(ATM):c.-111_-109delinsAC	rs1555051087
NM_000051.4(ATM):c.-74G>A	rs3205808

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