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Variant (rsID / SNP)

rs2243411

NAV2

rs2243411 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAV2. Location: chromosome 11, position 20,124,914. The table records no clinical significance for this variant.

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Reference-table entries

NAV2Not classified
Variant type
synonymous_variant
Chromosome / position
11:20124914
HGVS
NM_001244963.2,c.6708A>C,p.Gly2236Gly
Allele change
Synonymous_G2113G

Public references

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