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Variant (rsID / SNP)

rs6591595

MS4A13

rs6591595 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MS4A13. Location: chromosome 11, position 60,291,413. The table records no clinical significance for this variant.

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Reference-table entries

MS4A13Not classified
Variant type
missense_variant
Chromosome / position
11:60291413
HGVS
NM_001012417.3,c.173C>T,p.Pro58Leu
Allele change
Missense_P58L

Public references

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