Variant (rsID / SNP)

rs41266050

rs41266050 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RABGAP1L. Location: chromosome 1, position 174,516,999. The table records no clinical significance for this variant.

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Reference-table entries

RABGAP1LNot classified

Variant type: missense_variant
Chromosome / position: 1:174516999
HGVS: NM_001366445.1,c.1624C>T,p.Pro542Ser
Allele change: Silent

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.