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Variant (rsID / SNP)

rs2277582

IGDCC4

rs2277582 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGDCC4. Location: chromosome 15, position 65,684,533. The table records no clinical significance for this variant.

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Reference-table entries

IGDCC4Not classified
Variant type
synonymous_variant
Chromosome / position
15:65684533
HGVS
NM_020962.3,c.2061T>C,p.Ala687Ala
Allele change
Synonymous_A687A

Public references

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