Variant (rsID / SNP)

rs1801284

rs1801284 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGAP45. Location: chromosome 19, position 1,068,738. The table records no clinical significance for this variant.

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Reference-table entries

ARHGAP45Not classified

Variant type: missense_variant
Chromosome / position: 19:1068738
HGVS: NM_001258328.4,c.464G>A,p.Arg155His
Allele change: Missense_R155H

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.