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Variant (rsID / SNP)

rs2044693

PNO1

rs2044693 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PNO1. Location: chromosome 2, position 68,385,097. The table records no clinical significance for this variant.

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Reference-table entries

PNO1Not classified
Variant type
missense_variant
Chromosome / position
2:68385097
HGVS
NM_020143.4,c.31A>G,p.Arg11Gly
Allele change
Missense_R11G

Public references

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