Variant (rsID / SNP)

rs3827183

rs3827183 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOP1B. Location: chromosome 21, position 37,661,405. The table records no clinical significance for this variant.

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Reference-table entries

DOP1BNot classified

Variant type: missense_variant
Chromosome / position: 21:37661405
HGVS: NM_001320714.2,c.6416G>A,p.Gly2139Glu
Allele change: Missense_G2139E

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.