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Variant (rsID / SNP)

rs150075979

GJB6

rs150075979 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GJB6. Location: chromosome 13, position 20,797,605. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GJB6Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
13:20797605
Cytoband
13q12.11
HGVS
NM_001110219.3(GJB6):c.15G>A (p.Thr5=)
Allele change
Synonymous_T5T

Associated conditions / phenotypes

Hidrotic ectodermal dysplasia syndrome|Autosomal dominant nonsyndromic hearing loss 3B|Autosomal recessive nonsyndromic hearing loss 1A|Hidrotic ectodermal dysplasia syndrome|Autosomal recessive nonsyndromic hearing loss 1B

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.