List of variants in gene SLC9A6 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: 11

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 Xq26.3(chrX:135092601-135092742)x4
NM_001379110.1(SLC9A6):c.1159C>T (p.His387Tyr)	rs2148179162
NM_001379110.1(SLC9A6):c.1661+1G>A	rs796053283
NM_001379110.1(SLC9A6):c.1662-19_1662-3del	rs1569525894
NM_001379110.1(SLC9A6):c.442_444delinsC (p.Lys148fs)	rs2148149936
NM_001379110.1(SLC9A6):c.524+5G>A	rs796053284
NM_001379110.1(SLC9A6):c.55A>G (p.Ser19Gly)	rs2089324047
NM_001379110.1(SLC9A6):c.743+2dup	rs1603201598
NM_001379110.1(SLC9A6):c.743+3_743+6del	rs2148156632
NM_001379110.1(SLC9A6):c.886-1C>T
NM_001379110.1(SLC9A6):c.991G>C (p.Gly331Arg)	rs2148174022

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