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Variant (rsID / SNP)

rs3740015

DHTKD1

rs3740015 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DHTKD1. Location: chromosome 10, position 12,131,081. The table records no clinical significance for this variant.

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Reference-table entries

DHTKD1Not classified
Variant type
missense_variant
Chromosome / position
10:12131081
HGVS
NM_018706.7,c.814T>G,p.Tyr272Asp
Allele change
Missense_Y272D

Public references

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