List of variants in gene combination RELN, SLC26A5 reported as benign for lymphatic system disorder

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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: 31

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.*397G>A	rs7811262	0.99261
NM_005045.4(RELN):c.8843+7G>C	rs2711885	0.98938
NM_005045.4(RELN):c.10074A>G (p.Ala3358=)	rs1062831	0.17444
NM_005045.4(RELN):c.9443+45C>A	rs17151558	0.14621
NM_005045.4(RELN):c.8136A>G (p.Leu2712=)	rs3808039	0.04529
NM_005045.4(RELN):c.*151T>C	rs7811571	0.04492
NM_005045.4(RELN):c.8508C>T (p.Phe2836=)	rs2229862	0.03751
NM_005045.4(RELN):c.*67G>A	rs112874175	0.02333
NM_005045.4(RELN):c.10182-11G>A	rs57844600	0.01613
NM_005045.4(RELN):c.8950+16G>A	rs76565991	0.01546
NM_005045.4(RELN):c.9903C>T (p.Tyr3301=)	rs73714404	0.01371
NM_005045.4(RELN):c.*563C>A	rs150458916	0.00535
NM_005045.4(RELN):c.8811G>A (p.Ala2937=)	rs144728023	0.00226
NM_005045.4(RELN):c.9321C>T (p.Leu3107=)	rs150387973	0.00218
NM_005045.4(RELN):c.8120-9T>C	rs74952625	0.00190
NM_005045.4(RELN):c.8275-19T>C	rs149567032	0.00156
NM_005045.4(RELN):c.8944G>A (p.Asp2982Asn)	rs148509350	0.00071
NM_005045.4(RELN):c.9340A>G (p.Ile3114Val)	rs149613347	0.00031
NM_005045.4(RELN):c.10016T>C (p.Met3339Thr)	rs150638029	0.00019
NM_005045.4(RELN):c.10093G>A (p.Val3365Ile)	rs115035120	0.00018
NM_005045.4(RELN):c.8844-20T>C	rs142002220	0.00016
NM_005045.4(RELN):c.10322G>A (p.Arg3441Gln)	rs116463039	0.00011
NM_005045.4(RELN):c.10357C>T (p.Arg3453Ter)	rs139326865	0.00006
NM_005045.4(RELN):c.10266T>C (p.His3422=)
NM_005045.4(RELN):c.8120-9dup
NM_005045.4(RELN):c.8205T>C (p.His2735=)
NM_005045.4(RELN):c.8799T>C (p.Thr2933=)
NM_005045.4(RELN):c.8922C>T (p.Gly2974=)	rs544687307
NM_005045.4(RELN):c.9295AAG[1] (p.Lys3100del)	rs762015967
NM_005045.4(RELN):c.9370-13_9370-8del	rs141397961
NM_005045.4(RELN):c.9888G>A (p.Gly3296=)

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