Variant (rsID / SNP)

rs12896399

rs12896399 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC24A4, LOC105370627. Location: chromosome 14, position 92,773,663. Clinical significance in the table: association.

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Reference-table entries

SLC24A4Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 14:92773663
Cytoband: 14q32.12
HGVS: NC_000014.8:g.92773663G>T

Associated conditions / phenotypes

SKIN/HAIR/EYE PIGMENTATION 6, BLOND/BROWN HAIR

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.