List of variants in gene ADSL reported as likely benign for not specified

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_000026.4(ADSL):c.358-4G>A	rs113199851	0.01950
NM_000026.4(ADSL):c.440A>T (p.Lys147Met)	rs11089991	0.01397
NM_000026.4(ADSL):c.124C>T (p.Leu42=)	rs2228415	0.00969
NM_000026.4(ADSL):c.616G>T (p.Ala206Ser)	rs148411623	0.00155
NM_000026.4(ADSL):c.270T>C (p.Ala90=)	rs143275316	0.00039
NM_000026.4(ADSL):c.649C>G (p.His217Asp)	rs199761158	0.00024
NM_000026.4(ADSL):c.-37C>G	rs372357778	0.00012
NM_000026.4(ADSL):c.1102-16G>A	rs200428249	0.00010
NM_000026.4(ADSL):c.153+7G>A	rs376477242	0.00004
NM_000026.4(ADSL):c.153+11C>G	rs754451782	0.00003
NM_000026.4(ADSL):c.114A>G (p.Thr38=)	rs377588571	0.00002
NM_000026.4(ADSL):c.1191+16T>C	rs779771191	0.00001
NM_000026.4(ADSL):c.1369-17T>C	rs758511561	0.00001
NM_000026.4(ADSL):c.358-5C>T	rs769856337	0.00001
NM_000026.4(ADSL):c.42C>T (p.Arg14=)	rs768010749	0.00001
NM_000026.4(ADSL):c.75G>A (p.Glu25=)	rs1057522536	0.00001
NM_000026.4(ADSL):c.792+8G>T	rs777198113	0.00001
NM_000026.4(ADSL):c.793-5C>A	rs377164829	0.00001
NM_000026.4(ADSL):c.-8G>A	rs560389412
NM_000026.4(ADSL):c.1011-23_1011-20del	rs767894204
NM_000026.4(ADSL):c.1026C>T (p.Ala342=)	rs1280553241
NM_000026.4(ADSL):c.1191+11C>A	rs1057523739
NM_000026.4(ADSL):c.1272A>T (p.Ile424=)	rs1057522571
NM_000026.4(ADSL):c.1368+8del	rs758319423
NM_000026.4(ADSL):c.1369-7C>G	rs780296394
NM_000026.4(ADSL):c.403-11C>T	rs1057520899
NM_000026.4(ADSL):c.483-15T>C	rs1057520995
NM_000026.4(ADSL):c.558G>A (p.Leu186=)	rs1555907486
NM_000026.4(ADSL):c.863-20T>G	rs760407114
NM_000026.4(ADSL):c.9T>C (p.Ala3=)	rs758676257

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