Variant (rsID / SNP)

rs156962

rs156962 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLXNA4. Location: chromosome 7, position 132,192,949. The table records no clinical significance for this variant.

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Reference-table entries

PLXNA4Not classified

Variant type: synonymous_variant
Chromosome / position: 7:132192949
HGVS: NM_001393897.1,c.504A>G,p.Ser168Ser
Allele change: Synonymous_S168S

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.