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Variant (rsID / SNP)

rs2228628

ATF6B

rs2228628 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATF6B. Location: chromosome 6, position 32,088,854. The table records no clinical significance for this variant.

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Reference-table entries

ATF6BNot classified
Variant type
synonymous_variant
Chromosome / position
6:32088854
HGVS
NM_004381.5,c.612C>G,p.Ser204Ser
Allele change
Synonymous_S201S

Public references

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