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Variant (rsID / SNP)

rs1442710

NAV2

rs1442710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAV2. Location: chromosome 11, position 20,089,944. The table records no clinical significance for this variant.

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Reference-table entries

NAV2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
11:20089944
HGVS
NM_001244963.2,c.5151T>C,p.Asn1717Asn
Allele change
Synonymous_N1597N

Public references

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