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Variant (rsID / SNP)

rs925331

NECAB2

rs925331 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NECAB2. Location: chromosome 16, position 84,012,104. The table records no clinical significance for this variant.

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Reference-table entries

NECAB2Not classified
Variant type
missense_variant
Chromosome / position
16:84012104
HGVS
NM_001329749.2,c.59T>C,p.Leu20Ser
Allele change
Synonymous_L94L

Public references

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