Variant (rsID / SNP)

rs2671103

rs2671103 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLXNA4. Location: chromosome 7, position 131,815,310. The table records no clinical significance for this variant.

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Reference-table entries

PLXNA4Not classified

Variant type: synonymous_variant
Chromosome / position: 7:131815310
HGVS: NM_001393897.1,c.5613T>C,p.Asp1871Asp
Allele change: Synonymous_D1871D

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.