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Variant (rsID / SNP)

rs7499814

BANP

rs7499814 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BANP. Location: chromosome 16, position 88,052,161. The table records no clinical significance for this variant.

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Reference-table entries

BANPNot classified
Variant type
synonymous_variant
Chromosome / position
16:88052161
HGVS
NM_001386991.1,c.783C>A,p.Leu261Leu
Allele change
Synonymous_L222L

Associated conditions / phenotypes

Synonymous_L261L|Synonymous_L253L

Public references

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