Variant (rsID / SNP)

rs12422983

rs12422983 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAPGEF3. Location: chromosome 12, position 48,142,636. The table records no clinical significance for this variant.

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Reference-table entries

RAPGEF3Not classified

Variant type: missense_variant
Chromosome / position: 12:48142636
HGVS: NM_001098531.4,c.1120G>A,p.Gly374Ser
Allele change: Missense_G332S

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.