Variant (rsID / SNP)

rs3750534

rs3750534 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF183. Location: chromosome 9, position 116,060,124. The table records no clinical significance for this variant.

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Reference-table entries

RNF183Not classified

Variant type: missense_variant
Chromosome / position: 9:116060124
HGVS: NM_001371234.1,c.341A>G,p.Gln114Arg
Allele change: Missense_Q114R

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.