Variant (rsID / SNP)

rs3748357

rs3748357 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPGRIP1. Location: chromosome 14, position 21,785,790. The table records no clinical significance for this variant.

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Reference-table entries

RPGRIP1Not classified

Variant type: missense_variant
Chromosome / position: 14:21785790
HGVS: NM_001377523.1,c.13G>A,p.Asp5Asn
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.