Variant (rsID / SNP)

rs4781107

rs4781107 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC400499. Location: chromosome 16, position 11,572,419. The table records no clinical significance for this variant.

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Reference-table entries

LOC400499Not classified

Variant type: synonymous_variant
Chromosome / position: 16:11572419
HGVS: NM_001370704.1,c.2331T>G,p.Leu777Leu

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.