Variant (rsID / SNP)

rs11708527

rs11708527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RETNLB. Location: chromosome 3, position 108,475,974. The table records no clinical significance for this variant.

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Reference-table entries

RETNLBNot classified

Variant type: missense_variant
Chromosome / position: 3:108475974
HGVS: NM_032579.3,c.59C>T,p.Pro20Leu
Allele change: Missense_P20L

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.