Variant (rsID / SNP)

rs6042507

rs6042507 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIRPB2. Location: chromosome 20, position 1,459,060. The table records no clinical significance for this variant.

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Reference-table entries

SIRPB2Not classified

Variant type: missense_variant
Chromosome / position: 20:1459060
HGVS: NM_001122962.2,c.644A>C,p.Glu215Ala
Allele change: Missense_E117A

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.