List of variants in gene GDNF 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000514.4(GDNF):c.429G>A (p.Arg143=)	rs36010631	0.02743
NM_000514.4(GDNF):c.*988A>G	rs79669773	0.01403
NM_000514.4(GDNF):c.*1693G>T	rs188617599	0.00946
NM_000514.4(GDNF):c.*93A>T	rs45535335	0.00564
NM_000514.4(GDNF):c.*1406G>A	rs528922361	0.00328
NM_000514.4(GDNF):c.*2440G>A	rs78865769	0.00307
NM_000514.4(GDNF):c.277C>T (p.Arg93Trp)	rs36119840	0.00272
NM_000514.4(GDNF):c.*2150T>G	rs181589663	0.00263
NM_000514.4(GDNF):c.448G>A (p.Asp150Asn)	rs76466003	0.00230
NM_000514.4(GDNF):c.*1592G>T	rs546517198	0.00188
NM_000514.4(GDNF):c.*1276A>G	rs142426358	0.00150
NM_000514.4(GDNF):c.*1782G>A	rs147083416	0.00141
NM_000514.4(GDNF):c.*2014G>A	rs530864008	0.00114
NM_000514.4(GDNF):c.*5G>A	rs145996577	0.00045
NM_000514.4(GDNF):c.292G>T (p.Ala98Ser)	rs141837966	0.00029
NM_000514.4(GDNF):c.*1375T>C	rs566717310	0.00003
NM_000514.4(GDNF):c.*131GGA[10]	rs150577324
NM_000514.4(GDNF):c.-227CGG[6]	rs554953764

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