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Variant (rsID / SNP)

rs61746574

TPCN2

rs61746574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPCN2. Location: chromosome 11, position 68,840,399. The table records no clinical significance for this variant.

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Reference-table entries

TPCN2Not classified
Variant type
missense_variant
Chromosome / position
11:68840399
HGVS
NM_139075.4,c.1160G>A,p.Gly387Asp
Allele change
Missense_G387D

Public references

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