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Variant (rsID / SNP)

rs1104899

PM20D1

rs1104899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PM20D1. Location: chromosome 1, position 205,814,485. The table records no clinical significance for this variant.

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Reference-table entries

PM20D1Not classified
Variant type
missense_variant
Chromosome / position
1:205814485
HGVS
NM_152491.5,c.457C>T,p.Arg153Trp
Allele change
Missense_R153W

Public references

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