Variant (rsID / SNP)

rs5930932

rs5930932 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRG4. The table records no clinical significance for this variant.

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Reference-table entries

ADGRG4Not classified

Variant type: missense_variant
HGVS: NM_153834.4,c.5371T>C,p.Phe1791Leu
Allele change: Missense_F1791L

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.