Variant (rsID / SNP)

rs7278737

rs7278737 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LIPI. Location: chromosome 21, position 15,481,365. The table records no clinical significance for this variant.

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Reference-table entries

LIPINot classified

Variant type: missense_variant
Chromosome / position: 21:15481365
HGVS: NM_001302998.2,c.1332C>A,p.Asp444Glu
Allele change: Missense_T348K

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.