Variant (rsID / SNP)

rs1045922

rs1045922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNASE6. Location: chromosome 14, position 21,250,124. The table records no clinical significance for this variant.

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Reference-table entries

RNASE6Not classified

Variant type: missense_variant
Chromosome / position: 14:21250124
HGVS: NM_005615.5,c.266G>A,p.Arg89Gln
Allele change: Missense_R89Q

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.