List of variants in gene combination ATM, C11orf65 reported as pathogenic by Fulgent Genetics, Fulgent Genetics

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.5908C>T (p.Gln1970Ter)	rs587781722	0.00021
NM_000051.4(ATM):c.7271T>G (p.Val2424Gly)	rs28904921	0.00006
NM_000051.4(ATM):c.5763-1050A>G	rs774925473	0.00004
NM_000051.4(ATM):c.5932G>T (p.Glu1978Ter)	rs587779852	0.00004
NM_000051.4(ATM):c.8147T>C (p.Val2716Ala)	rs587782652	0.00004
NM_000051.4(ATM):c.8786+1G>A	rs17174393	0.00002
NM_000051.4(ATM):c.6095G>A (p.Arg2032Lys)	rs139770721	0.00001
NM_000051.4(ATM):c.6679C>T (p.Arg2227Cys)	rs564652222	0.00001
NM_000051.4(ATM):c.6997dup	rs587781299	0.00001
NM_000051.4(ATM):c.7630-2A>C	rs587779866	0.00001
NM_000051.4(ATM):c.8266A>T (p.Lys2756Ter)	rs371638537	0.00001
NM_000051.4(ATM):c.8988-1G>C	rs730881386	0.00001
NM_000051.4(ATM):c.9139C>T (p.Arg3047Ter)	rs121434219	0.00001
NM_000051.4(ATM):c.6200C>A (p.Ala2067Asp)	rs397514577
NM_000051.4(ATM):c.6326G>A (p.Trp2109Ter)	rs587782114
NM_000051.4(ATM):c.6615G>A (p.Trp2205Ter)	rs1555119041
NM_000051.4(ATM):c.7792C>T (p.Arg2598Ter)	rs138941496
NM_000051.4(ATM):c.8851-1G>T	rs1057516537
NM_000051.4(ATM):c.8977C>T (p.Arg2993Ter)	rs770641163

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