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Variant (rsID / SNP)

rs10803570

NXPH2

rs10803570 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NXPH2. Location: chromosome 2, position 139,429,068. The table records no clinical significance for this variant.

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Reference-table entries

NXPH2Not classified
Variant type
synonymous_variant
Chromosome / position
2:139429068
HGVS
NM_007226.3,c.219C>T,p.Tyr73Tyr
Allele change
Synonymous_Y73Y

Public references

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