Variant (rsID / SNP)

rs11544145

rs11544145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPP30. Location: chromosome 10, position 92,631,778. The table records no clinical significance for this variant.

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Reference-table entries

RPP30Not classified

Variant type: missense_variant
Chromosome / position: 10:92631778
HGVS: NM_001104546.2,c.35G>A,p.Gly12Asp
Allele change: Missense_G12D

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.