Variant (rsID / SNP)

rs3803650

rs3803650 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC7A6OS, PRMT7. Location: chromosome 16, position 68,344,696. The table records no clinical significance for this variant.

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Reference-table entries

SLC7A6OSNot classified

Variant type: missense_variant
Chromosome / position: 16:68344696
HGVS: NM_032178.3,c.134G>A,p.Gly45Asp
Allele change: Missense_G45D

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.