Variant (rsID / SNP)

rs28564871

rs28564871 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABHD12B. Location: chromosome 14, position 51,368,610. The table records no clinical significance for this variant.

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Reference-table entries

ABHD12BNot classified

Variant type: missense_variant
Chromosome / position: 14:51368610
HGVS: NM_001206673.2,c.844A>G,p.Ile282Val
Allele change: Missense_I175V

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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