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Variant (rsID / SNP)

rs6702754

ATP8B2

rs6702754 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP8B2. Location: chromosome 1, position 154,303,976. The table records no clinical significance for this variant.

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Reference-table entries

ATP8B2Not classified
Variant type
synonymous_variant
Chromosome / position
1:154303976
HGVS
NM_001367934.1,c.417T>C,p.Asn139Asn
Allele change
Synonymous_N120N

Public references

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