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Variant (rsID / SNP)

rs2295612

SLAMF1

rs2295612 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLAMF1. Location: chromosome 1, position 160,616,703. The table records no clinical significance for this variant.

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Reference-table entries

SLAMF1Not classified
Variant type
missense_variant
Chromosome / position
1:160616703
HGVS
NM_001330754.2,c.33C>A,p.Phe11Leu
Allele change
Missense_F11L

Public references

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