Variant (rsID / SNP)

rs6683071

rs6683071 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM177B. Location: chromosome 1, position 222,923,351. The table records no clinical significance for this variant.

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Reference-table entries

FAM177BNot classified

Variant type: missense_variant
Chromosome / position: 1:222923351
HGVS: NM_001324080.2,c.428A>G,p.Gln143Arg
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.