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Variant (rsID / SNP)

rs12363342

MS4A15

rs12363342 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MS4A15. Location: chromosome 11, position 60,531,264. The table records no clinical significance for this variant.

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Reference-table entries

MS4A15Not classified
Variant type
missense_variant
Chromosome / position
11:60531264
HGVS
NM_001098835.2,c.58A>G,p.Ser20Gly
Allele change
Silent

Public references

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