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Variant (rsID / SNP)

rs1137930

PNO1

rs1137930 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PNO1. Location: chromosome 2, position 68,388,823. The table records no clinical significance for this variant.

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Reference-table entries

PNO1Not classified
Variant type
synonymous_variant
Chromosome / position
2:68388823
HGVS
NM_020143.4,c.366A>G,p.Lys122Lys
Allele change
Synonymous_K122K

Public references

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