Variant (rsID / SNP)

rs62525422

rs62525422 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRCC1. Location: chromosome 8, position 86,021,994. The table records no clinical significance for this variant.

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Reference-table entries

LRRCC1Not classified

Variant type: missense_variant
Chromosome / position: 8:86021994
HGVS: NM_033402.5,c.269G>A,p.Cys90Tyr
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.