Variant (rsID / SNP)

rs1128397

rs1128397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFRA2. Location: chromosome 8, position 21,550,800. The table records no clinical significance for this variant.

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Reference-table entries

GFRA2Not classified

Variant type: missense_variant
Chromosome / position: 8:21550800
HGVS: NM_001495.5,c.1385T>A,p.Leu462Gln
Allele change: Missense_L329Q

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.