Variant (rsID / SNP)

rs908828

rs908828 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA2. Location: chromosome 9, position 139,913,239. The table records no clinical significance for this variant.

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Reference-table entries

ABCA2Not classified

Variant type: missense_variant
Chromosome / position: 9:139913239
HGVS: NM_212533.3,c.1841A>C,p.His614Pro
Allele change: Missense_H614P

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.