Variant (rsID / SNP)

rs2130882

rs2130882 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARRDC4. Location: chromosome 15, position 98,513,845. The table records no clinical significance for this variant.

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Reference-table entries

ARRDC4Not classified

Variant type: missense_variant
Chromosome / position: 15:98513845
HGVS: NM_183376.3,c.1072T>C,p.Ser358Pro
Allele change: Missense_S358P

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.