Variants in gene POMT2 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_013382.7(POMT2):c.1935C>T (p.Leu645=)	rs141193672	0.00066
NM_013382.7(POMT2):c.649G>A (p.Ala217Thr)	rs144748043	0.00065
NM_013382.7(POMT2):c.1701C>G (p.Pro567=)	rs151051452	0.00062
NM_013382.7(POMT2):c.1903G>A (p.Val635Ile)	rs142299878	0.00061
NM_013382.7(POMT2):c.229G>A (p.Asp77Asn)	rs200992827	0.00051
NM_013382.7(POMT2):c.1404A>G (p.Lys468=)	rs150491326	0.00043
NM_013382.7(POMT2):c.66C>T (p.Gly22=)	rs200670377	0.00027
NM_013382.7(POMT2):c.806G>A (p.Ser269Asn)	rs375217032	0.00026
NM_013382.7(POMT2):c.1206A>C (p.Pro402=)	rs142479943	0.00016
NM_013382.7(POMT2):c.1920C>T (p.Gly640=)	rs150755807	0.00013
NM_013382.7(POMT2):c.1250A>G (p.Lys417Arg)	rs147268052	0.00011
NM_013382.7(POMT2):c.2057G>A (p.Arg686Gln)	rs200163818	0.00005
NM_013382.7(POMT2):c.1017C>T (p.Tyr339=)	rs1026361359	0.00004
NM_013382.7(POMT2):c.1743G>A (p.Gly581=)	rs755254043	0.00003
NM_013382.7(POMT2):c.1654-8T>G	rs780532724	0.00002
NM_013382.7(POMT2):c.629T>C (p.Met210Thr)	rs369654108	0.00001
NM_013382.7(POMT2):c.651C>T (p.Ala217=)	rs147845081	0.00001
NM_013382.7(POMT2):c.1726-9A>T	rs747493997
NM_013382.7(POMT2):c.232G>C (p.Glu78Gln)	rs151103906

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