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Variant (rsID / SNP)

rs837550

LPCAT2

rs837550 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPCAT2. Location: chromosome 16, position 55,562,466. The table records no clinical significance for this variant.

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Reference-table entries

LPCAT2Not classified
Variant type
missense_variant
Chromosome / position
16:55562466
HGVS
NM_017839.5,c.489G>A,p.Met163Ile
Allele change
Missense_M163I

Public references

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