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Variant (rsID / SNP)

rs2048074

NEIL3

rs2048074 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEIL3. Location: chromosome 4, position 178,274,565. The table records no clinical significance for this variant.

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Reference-table entries

NEIL3Not classified
Variant type
synonymous_variant
Chromosome / position
4:178274565
HGVS
NM_018248.3,c.1143A>G,p.Arg381Arg
Allele change
Synonymous_R381R

Public references

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