Variant (rsID / SNP)

rs2731038

rs2731038 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DBX2. Location: chromosome 12, position 45,417,666. The table records no clinical significance for this variant.

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Reference-table entries

DBX2Not classified

Variant type: missense_variant
Chromosome / position: 12:45417666
HGVS: NM_001004329.3,c.511A>G,p.Met171Val
Allele change: Missense_M171V

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.