Variant (rsID / SNP)

rs6702823

rs6702823 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNST. Location: chromosome 1, position 246,755,124. The table records no clinical significance for this variant.

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Reference-table entries

CNSTNot classified

Variant type: missense_variant
Chromosome / position: 1:246755124
HGVS: NM_152609.3,c.260T>C,p.Leu87Ser
Allele change: Missense_L87S

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.