Variant (rsID / SNP)

rs6505776

rs6505776 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEH1L. Location: chromosome 18, position 12,984,144. The table records no clinical significance for this variant.

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Reference-table entries

SEH1LNot classified

Variant type: missense_variant
Chromosome / position: 18:12984144
HGVS: NM_001013437.2,c.1025C>A,p.Thr342Asn
Allele change: Missense_T342N

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.