Variant (rsID / SNP)

rs12203592

rs12203592 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IRF4. Location: chromosome 6, position 396,321. Clinical significance in the table: Affects.

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Reference-table entries

IRF4Other

Clinical significance (as recorded): Affects
Variant type: single nucleotide variant
Chromosome / position: 6:396321
Cytoband: 6p25.3
HGVS: NM_002460.4(IRF4):c.492+386C>T
Allele change: Silent

Associated conditions / phenotypes

Skin/hair/eye pigmentation, variation in, 8

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.