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Variant (rsID / SNP)

rs61735719

GPR39

rs61735719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR39. Location: chromosome 2, position 133,402,949. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GPR39Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:133402949
Cytoband
2q21.2
HGVS
NM_001508.3(GPR39):c.1132G>A (p.Ala378Thr)
Allele change
Missense_A378T

Public references

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