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Variant (rsID / SNP)

rs1127000

PLXNB2

rs1127000 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLXNB2. Location: chromosome 22, position 50,716,167. The table records no clinical significance for this variant.

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Reference-table entries

PLXNB2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
22:50716167
HGVS
NM_001376864.1,c.5286C>T,p.Ser1762Ser
Allele change
Synonymous_S1683S

Public references

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