Variant (rsID / SNP)

rs642742

rs642742 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KITLG. Location: chromosome 12, position 89,299,746. Clinical significance in the table: Affects.

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Reference-table entries

KITLGOther

Clinical significance (as recorded): Affects
Variant type: single nucleotide variant
Chromosome / position: 12:89299746
Cytoband: 12q21.33
HGVS: NC_000012.12:g.88905969C>T

Associated conditions / phenotypes

SKIN/HAIR/EYE PIGMENTATION 7, DARK/LIGHT SKIN

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.