Variant (rsID / SNP)

rs4907817

rs4907817 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLRA4. The table records no clinical significance for this variant.

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Reference-table entries

GLRA4Not classified

Variant type: non_coding_transcript_exon_variant
HGVS: NR_164162.1,n.545A>G
Allele change: Missense_I85V

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.