Variant (rsID / SNP)

rs10108545

rs10108545 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCM1. Location: chromosome 8, position 17,799,241. The table records no clinical significance for this variant.

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Reference-table entries

PCM1Not classified

Variant type: intron_variant
Chromosome / position: 8:17799241
HGVS: NM_001352632.2,c.900+1574T>C
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.