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Variant (rsID / SNP)

rs28379706

PLXNB2

rs28379706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLXNB2. Location: chromosome 22, position 50,728,062. The table records no clinical significance for this variant.

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Reference-table entries

PLXNB2Not classified
Variant type
missense_variant
Chromosome / position
22:50728062
HGVS
NM_001376864.1,c.952A>G,p.Lys318Glu
Allele change
Missense_K318E

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.