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Variant (rsID / SNP)

rs2076185

ADTRP

rs2076185 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADTRP. Location: chromosome 6, position 11,723,636. The table records no clinical significance for this variant.

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Reference-table entries

ADTRPNot classified
Variant type
missense_variant
Chromosome / position
6:11723636
HGVS
NM_001143948.2,c.658G>A,p.Val220Ile
Allele change
Missense_V220I

Public references

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