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Variant (rsID / SNP)

rs2376558

TPCN2

rs2376558 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPCN2. Location: chromosome 11, position 68,851,414. The table records no clinical significance for this variant.

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Reference-table entries

TPCN2Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
11:68851414
HGVS
NM_139075.4,c.1691T>C,p.Leu564Pro
Allele change
Missense_L564P

Public references

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