Variant (rsID / SNP)

rs1891460

rs1891460 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PM20D1. Location: chromosome 1, position 205,814,497. The table records no clinical significance for this variant.

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Reference-table entries

PM20D1Not classified

Variant type: missense_variant
Chromosome / position: 1:205814497
HGVS: NM_152491.5,c.445A>G,p.Ile149Val
Allele change: Missense_I149V

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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