Variant (rsID / SNP)

rs200964994

rs200964994 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOMER2. Location: chromosome 15, position 83,523,438. Clinical significance in the table: Uncertain significance.

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Reference-table entries

HOMER2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:83523438
Cytoband: 15q25.2
HGVS: NM_004839.4(HOMER2):c.609G>T (p.Gln203His)
Allele change: Missense_Q214H

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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