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Variant (rsID / SNP)

rs2052937

ADGRF3

rs2052937 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRF3. Location: chromosome 2, position 26,536,694. The table records no clinical significance for this variant.

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Reference-table entries

ADGRF3Not classified
Variant type
missense_variant
Chromosome / position
2:26536694
HGVS
NM_001145168.1,c.1210G>A,p.Ala404Thr
Allele change
Missense_A205T

Associated conditions / phenotypes

Missense_A404T

Public references

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