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Variant (rsID / SNP)

rs8107776

NWD1

rs8107776 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NWD1. Location: chromosome 19, position 16,842,052. The table records no clinical significance for this variant.

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Reference-table entries

NWD1Not classified
Variant type
missense_variant
Chromosome / position
19:16842052
HGVS
NM_001007525.5,c.44G>T,p.Cys15Phe
Allele change
Missense_C15F

Public references

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