Variants in gene SLC4A1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000342.3(SLC4A1):c.1462G>A (p.Val488Met)	rs28931584	0.00001
NM_000342.4(SLC4A1):c.1468C>T (p.Arg490Cys)	rs1398477044	0.00001
NM_000342.3(SLC4A1):c.2279G>A (p.Arg760Gln)	rs121912755
NM_000342.3(SLC4A1):c.2608C>T (p.Arg870Trp)	rs28931585
NM_000342.4(SLC4A1):c.1030C>T (p.Arg344Ter)	rs750930293
NM_000342.4(SLC4A1):c.1353_1380del (p.Phe451fs)
NM_000342.4(SLC4A1):c.1561C>T (p.Gln521Ter)	rs2144612096
NM_000342.4(SLC4A1):c.16-1G>A
NM_000342.4(SLC4A1):c.1765C>T (p.Arg589Cys)	rs121912745
NM_000342.4(SLC4A1):c.184C>T (p.Gln62Ter)
NM_000342.4(SLC4A1):c.1890+1G>A	rs1567830555
NM_000342.4(SLC4A1):c.202G>T (p.Glu68Ter)	rs13306787
NM_000342.4(SLC4A1):c.2057+1G>A	rs2047371081
NM_000342.4(SLC4A1):c.2169G>A (p.Trp723Ter)	rs2047358814
NM_000342.4(SLC4A1):c.2188C>T (p.Arg730Cys)	rs770569237
NM_000342.4(SLC4A1):c.2214_2217del (p.Thr739fs)
NM_000342.4(SLC4A1):c.2278C>T (p.Arg760Trp)	rs373916826
NM_000342.4(SLC4A1):c.2423G>A (p.Arg808His)	rs866727908
NM_000342.4(SLC4A1):c.2510C>T (p.Thr837Met)	rs2047337144
NM_000342.4(SLC4A1):c.2573C>A (p.Ala858Asp)	rs121912751
NM_000342.4(SLC4A1):c.349+1G>A	rs1567834739
NM_000342.4(SLC4A1):c.609+1G>A	rs1362663440

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