Variant (rsID / SNP)

rs12819884

rs12819884 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GDF3. Location: chromosome 12, position 7,842,932. The table records no clinical significance for this variant.

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Reference-table entries

GDF3Not classified

Variant type: missense_variant
Chromosome / position: 12:7842932
HGVS: NM_020634.3,c.637G>A,p.Gly213Arg
Allele change: Missense_G213R

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.