Variants in gene F11 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.809A>T (p.Lys270Ile)	rs121965070	0.00055
NM_000128.4(F11):c.400C>T (p.Gln134Ter)	rs756908183	0.00004
NM_000128.4(F11):c.422C>T (p.Thr141Met)	rs200593979	0.00004
NM_000128.4(F11):c.723C>G (p.Phe241Leu)	rs281875265	0.00004
NM_000128.4(F11):c.325G>A (p.Ala109Thr)	rs768474112	0.00002
NM_000128.4(F11):c.1103G>C (p.Gly368Ala)	rs748926718	0.00001
NM_000128.4(F11):c.1546G>A (p.Val516Met)	rs200622588	0.00001
NM_000128.4(F11):c.1789G>A (p.Glu597Lys)	rs281875251	0.00001
NM_000128.4(F11):c.302A>G (p.Lys101Arg)	rs281875272	0.00001
NM_000128.4(F11):c.599G>A (p.Cys200Tyr)	rs757817254	0.00001
NM_000128.4(F11):c.1288G>T (p.Ala430Ser)
NM_000128.4(F11):c.1481-1G>T	rs1057516506
NM_000128.4(F11):c.218+4A>G	rs767240420
NM_000128.4(F11):c.449C>T (p.Thr150Met)	rs1340928778
NM_000128.4(F11):c.977G>A (p.Arg326His)	rs1554082932
Single allele

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