Variant (rsID / SNP)

rs2286586

rs2286586 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MXRA7. Location: chromosome 17, position 74,684,452. The table records no clinical significance for this variant.

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Reference-table entries

MXRA7Not classified

Variant type: missense_variant
Chromosome / position: 17:74684452
HGVS: NM_001387276.1,c.278C>T,p.Pro93Leu
Allele change: Silent

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.