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Variant (rsID / SNP)

rs36077496

FRZB

rs36077496 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FRZB. Location: chromosome 2, position 183,731,193. The table records no clinical significance for this variant.

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Reference-table entries

FRZBNot classified
Variant type
missense_variant
Chromosome / position
2:183731193
HGVS
NM_001463.4,c.88G>T,p.Ala30Ser
Allele change
Missense_A30S

Public references

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