Variant (rsID / SNP)

rs8021664

rs8021664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPC2, SYNDIG1L. Location: chromosome 14, position 74,943,295. The table records no clinical significance for this variant.

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Reference-table entries

NPC2Not classified

Variant type: downstream_gene_variant
Chromosome / position: 14:74943295
HGVS: NM_001363688.1,c.*4026A>G

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.