Variant (rsID / SNP)

rs916977

rs916977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HERC2. Location: chromosome 15, position 28,513,364. Clinical significance in the table: Affects.

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Reference-table entries

HERC2Other

Clinical significance (as recorded): Affects
Variant type: single nucleotide variant
Chromosome / position: 15:28513364
Cytoband: 15q13.1
HGVS: NM_004667.6(HERC2):c.1598+247A>G
Allele change: Silent

Associated conditions / phenotypes

Skin/hair/eye pigmentation, variation in, 1

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.