Variant (rsID / SNP)

rs2233952

rs2233952 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSORS1C2, PSORS1C1. Location: chromosome 6, position 31,105,891. The table records no clinical significance for this variant.

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Reference-table entries

PSORS1C2Not classified

Variant type: missense_variant
Chromosome / position: 6:31105891
HGVS: NM_014069.3,c.248T>C,p.Leu83Pro
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.