Variant (rsID / SNP)

rs13112390

rs13112390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEIL3. Location: chromosome 4, position 178,274,835. The table records no clinical significance for this variant.

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Reference-table entries

NEIL3Not classified

Variant type: missense_variant
Chromosome / position: 4:178274835
HGVS: NM_018248.3,c.1413A>C,p.Gln471His
Allele change: Missense_Q471H

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.