Variant (rsID / SNP)

rs1211554

rs1211554 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HUS1B, EXOC2. Location: chromosome 6, position 656,143. The table records no clinical significance for this variant.

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Reference-table entries

HUS1BNot classified

Variant type: missense_variant
Chromosome / position: 6:656143
HGVS: NM_148959.4,c.802G>T,p.Asp268Tyr
Allele change: Silent

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.