Variant (rsID / SNP)

rs16862653

rs16862653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NBAS. Location: chromosome 2, position 15,542,352. The table records no clinical significance for this variant.

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Reference-table entries

NBASNot classified

Variant type: missense_variant
Chromosome / position: 2:15542352
HGVS: NM_015909.4,c.3011G>A,p.Arg1004Gln
Allele change: Silent

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.