Variant (rsID / SNP)

rs12051468

rs12051468 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRISPLD2. Location: chromosome 16, position 84,879,464. The table records no clinical significance for this variant.

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Reference-table entries

CRISPLD2Not classified

Variant type: missense_variant
Chromosome / position: 16:84879464
HGVS: NM_031476.4,c.313A>G,p.Ser105Gly
Allele change: Missense_S105G

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.