List of variants in gene GDAP1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_018972.4(GDAP1):c.*1489del	rs34856543	0.04395
NM_018972.4(GDAP1):c.*2408G>A	rs11996204	0.02523
NM_018972.4(GDAP1):c.*1162T>C	rs113017051	0.00611
NM_018972.4(GDAP1):c.*723G>A	rs116863614	0.00512
NM_018972.4(GDAP1):c.*1819T>C	rs141157275	0.00466
NM_018972.4(GDAP1):c.*1006C>T	rs145523828	0.00367
NM_018972.4(GDAP1):c.*1701T>C	rs781146378	0.00025
NM_018972.4(GDAP1):c.*1639A>G	rs145245478
NM_018972.4(GDAP1):c.*1639A>T	rs145245478
NM_018972.4(GDAP1):c.-51_-49del	rs201803887

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