ClinVar Miner

List of variants in gene SLC9A6 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 Xq26.3(chrX:135092601-135092742)x4
NM_001379110.1(SLC9A6):c.1661+1G>A rs796053283
NM_001379110.1(SLC9A6):c.442_444delinsC (p.Lys148fs) rs2148149936
NM_001379110.1(SLC9A6):c.743+2dup rs1603201598
NM_001379110.1(SLC9A6):c.991G>C (p.Gly331Arg) rs2148174022

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