List of variants in gene SLC9A6 reported as 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001379110.1(SLC9A6):c.1143_1144del (p.Phe382fs)	rs1064793575
NM_001379110.1(SLC9A6):c.1224_1230delinsGTCTTGGGAAGAGCT (p.Asn408fs)	rs1556620027
NM_001379110.1(SLC9A6):c.1342C>T (p.Arg448Ter)	rs122461162
NM_001379110.1(SLC9A6):c.1438dup (p.Met480fs)	rs2148190013
NM_001379110.1(SLC9A6):c.1570C>T (p.Gln524Ter)	rs2521409119
NM_001379110.1(SLC9A6):c.1661+1G>A	rs796053283
NM_001379110.1(SLC9A6):c.190dup (p.Leu64fs)	rs796053293
NM_001379110.1(SLC9A6):c.448-1G>A	rs797044508
NM_001379110.1(SLC9A6):c.459dup (p.Arg154fs)
NM_001379110.1(SLC9A6):c.460C>T (p.Arg154Ter)
NM_001379110.1(SLC9A6):c.743+1G>A	rs1556617455
NM_001379110.1(SLC9A6):c.743+3_743+6del	rs2148156632
NM_001379110.1(SLC9A6):c.797_798del (p.Thr266fs)	rs796053297
NM_001379110.1(SLC9A6):c.916C>T (p.Gln306Ter)	rs398124224
NM_006359.2(SLC9A6):c.509_510delGA	rs1064795183
NM_006359.2(SLC9A6):c.585dupG	rs796053291

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