Variant (rsID / SNP)

rs145122087

rs145122087 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC728392. Location: chromosome 17, position 5,404,152. The table records no clinical significance for this variant.

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Reference-table entries

LOC728392Not classified

Variant type: missense_variant
Chromosome / position: 17:5404152
HGVS: NM_001162371.3,c.125C>T,p.Ser42Leu
Allele change: Missense_S42L

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.