List of variants in gene SIN3A reported as likely pathogenic for not provided

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001145358.2(SIN3A):c.1366dup (p.Ser456fs)	rs1595904430
NM_001145358.2(SIN3A):c.1527-2A>C
NM_001145358.2(SIN3A):c.1657C>T (p.Arg553Ter)	rs1555444885
NM_001145358.2(SIN3A):c.1738-1G>A	rs1555444809
NM_001145358.2(SIN3A):c.1846C>T (p.Arg616Cys)	rs2073382517
NM_001145358.2(SIN3A):c.1855-13_1874inv
NM_001145358.2(SIN3A):c.1885A>G (p.Thr629Ala)
NM_001145358.2(SIN3A):c.2094-1G>A
NM_001145358.2(SIN3A):c.2277+4A>G	rs1555444022
NM_001145358.2(SIN3A):c.2844_2847del (p.Lys948fs)	rs1555443581
NM_001145358.2(SIN3A):c.3199_3207dup (p.Met1067_Ile1069dup)	rs2072974210
NM_001145358.2(SIN3A):c.3303C>G (p.Tyr1101Ter)	rs778623853
NM_001145358.2(SIN3A):c.3409C>T (p.Gln1137Ter)	rs2072844502
NM_001145358.2(SIN3A):c.367-2A>C
NM_001145358.2(SIN3A):c.481A>G (p.Thr161Ala)

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