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Variant (rsID / SNP)

rs9369738

ADGRF4

rs9369738 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRF4. Location: chromosome 6, position 47,682,604. The table records no clinical significance for this variant.

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Reference-table entries

ADGRF4Not classified
Variant type
missense_variant
Chromosome / position
6:47682604
HGVS
NM_001347855.2,c.1623A>C,p.Lys541Asn
Allele change
Missense_K541N

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.