List of variants in gene C12orf57 reported as benign by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
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: 10

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HGVS	dbSNP	gnomAD frequency
NM_138425.4(C12orf57):c.230-75G>A	rs2019743	0.98791
NM_138425.4(C12orf57):c.52+26A>G	rs915997	0.88408
NM_138425.4(C12orf57):c.229+93C>T	rs744167	0.19044
NM_138425.4(C12orf57):c.229+145C>T	rs73262868	0.02153
NM_138425.4(C12orf57):c.-70T>G	rs114366875	0.01732
NM_001301834.1(C12orf57):c.-16+153G>A	rs61917871
NM_138425.3(C12orf57):c.-136A>C	rs1044189
NM_138425.3(C12orf57):c.-164G>A	rs112885868
NM_138425.3(C12orf57):c.-189T>C	rs74057227
NM_138425.3(C12orf57):c.-200A>G	rs3087835

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