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Variant (rsID / SNP)

rs2305243

ATL2

rs2305243 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATL2. Location: chromosome 2, position 38,536,626. The table records no clinical significance for this variant.

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Reference-table entries

ATL2Not classified
Variant type
synonymous_variant
Chromosome / position
2:38536626
HGVS
NM_001330463.2,c.966A>C,p.Arg322Arg
Allele change
Synonymous_R304R

Associated conditions / phenotypes

Synonymous_R322R|Synonymous_R95R|Synonymous_R322R|Synonymous_R151R|Synonymous_R322R

Public references

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