Variants in gene ANKRD11 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
NM_013275.6(ANKRD11):c.6112A>G (p.Lys2038Glu)	rs200724087	0.00045
NM_013275.6(ANKRD11):c.6919C>T (p.Pro2307Ser)	rs575642464	0.00035
NM_013275.6(ANKRD11):c.1133A>G (p.Asn378Ser)	rs202203523	0.00034
NM_013275.6(ANKRD11):c.7714-3C>A	rs199741062	0.00026
NM_013275.6(ANKRD11):c.6580C>G (p.Gln2194Glu)	rs201589586	0.00023
NM_013275.6(ANKRD11):c.116C>T (p.Thr39Ile)	rs149152296	0.00022
NM_013275.6(ANKRD11):c.3274C>T (p.Pro1092Ser)	rs773172347	0.00011
NM_013275.6(ANKRD11):c.1360G>A (p.Val454Met)	rs149569330	0.00008
NM_013275.6(ANKRD11):c.3953C>G (p.Thr1318Ser)	rs570483616	0.00008
NM_013275.6(ANKRD11):c.301G>A (p.Gly101Arg)	rs1373571533	0.00002
NM_013275.6(ANKRD11):c.3418G>A (p.Ala1140Thr)	rs369869329	0.00001
NM_013275.6(ANKRD11):c.3467G>A (p.Arg1156Gln)	rs775910970	0.00001
NM_013275.6(ANKRD11):c.1652_1666del (p.Trp551_Ser555del)	rs780150752
NM_013275.6(ANKRD11):c.6115G>A (p.Asp2039Asn)

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