Variant (rsID / SNP)

rs7474140

rs7474140 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RTL4. The table records no clinical significance for this variant.

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Reference-table entries

RTL4Not classified

Variant type: missense_variant
HGVS: NM_001004308.3,c.484G>T,p.Asp162Tyr
Allele change: Missense_D162Y

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.