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Variant (rsID / SNP)

rs2147896

PYROXD2

rs2147896 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PYROXD2. Location: chromosome 10, position 100,148,176. The table records no clinical significance for this variant.

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Reference-table entries

PYROXD2Not classified
Variant type
missense_variant
Chromosome / position
10:100148176
HGVS
NM_032709.3,c.1382T>C,p.Met461Thr
Allele change
Missense_M461T

Public references

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