Variant (rsID / SNP)

rs3961799

LOC105372077

rs3961799 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC105372077. The table records no clinical significance for this variant.

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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.