Variant (rsID / SNP)

rs73302786

rs73302786 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM170B. Location: chromosome 10, position 50,339,754. The table records no clinical significance for this variant.

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Reference-table entries

FAM170BNot classified

Variant type: missense_variant
Chromosome / position: 10:50339754
HGVS: NM_001164484.2,c.756C>A,p.Asp252Glu
Allele change: Silent

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.