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Variant (rsID / SNP)

rs34356735

LHX3

rs34356735 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LHX3. Location: chromosome 9, position 139,091,521. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LHX3Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
9:139091521
Cytoband
9q34.3
HGVS
NM_178138.6(LHX3):c.454+3C>T
Allele change
Silent

Associated conditions / phenotypes

Non-acquired combined pituitary hormone deficiency with spine abnormalities|Combined pituitary hormone deficiencies, genetic form

Public references

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