Variant (rsID / SNP)

rs2275575

rs2275575 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTARC2. Location: chromosome 1, position 220,935,081. The table records no clinical significance for this variant.

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Reference-table entries

MTARC2Not classified

Variant type: synonymous_variant
Chromosome / position: 1:220935081
HGVS: NM_001317338.2,c.528G>A,p.Ala176Ala
Allele change: Synonymous_A176A

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.