Variant (rsID / SNP)

rs6568050

rs6568050 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.80T>C,p.Leu27Pro
Allele change: Missense_L27P

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.