Variant (rsID / SNP)

rs2301770

rs2301770 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERI2, ACSM3. Location: chromosome 16, position 20,802,172. The table records no clinical significance for this variant.

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Reference-table entries

ERI2Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 16:20802172
HGVS: NM_080663.3,c.815G>A,p.Gly272Asp
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.