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Variant (rsID / SNP)

rs3744877

ADNP2

rs3744877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADNP2. Location: chromosome 18, position 77,894,844. The table records no clinical significance for this variant.

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Reference-table entries

ADNP2Not classified
Variant type
synonymous_variant
Chromosome / position
18:77894844
HGVS
NM_014913.4,c.1548G>A,p.Pro516Pro
Allele change
Synonymous_P516P

Public references

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