List of variants in gene combination BRCA1, LOC126862571 reported as uncertain significance for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3649T>C (p.Ser1217Pro)	rs273900712	0.00008
NM_007294.4(BRCA1):c.3758C>G (p.Ser1253Cys)	rs397509100	0.00004
NM_007294.4(BRCA1):c.3403C>G (p.Gln1135Glu)	rs80357136
NM_007294.4(BRCA1):c.3424G>C (p.Ala1142Pro)	rs80357101
NM_007294.4(BRCA1):c.3555G>T (p.Glu1185Asp)	rs587779368
NM_007294.4(BRCA1):c.3769GAG[1] (p.Glu1258del)	rs1057517536
NM_007294.4(BRCA1):c.4001G>A (p.Gly1334Asp)	rs2053486938
NM_007294.4(BRCA1):c.4096+3A>G	rs80358015

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