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Variant (rsID / SNP)

rs1970817

ATF7IP2

rs1970817 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATF7IP2. Location: chromosome 16, position 10,575,824. The table records no clinical significance for this variant.

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Reference-table entries

ATF7IP2Not classified
Variant type
synonymous_variant
Chromosome / position
16:10575824
HGVS
NM_001352120.2,c.1767C>A,p.Pro589Pro
Allele change
Silent

Public references

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