Variant (rsID / SNP)

rs61734970

rs61734970 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM20C. Location: chromosome 7, position 195,594. Clinical significance in the table: Benign.

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Reference-table entries

FAM20CBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:195594
Cytoband: 7p22.3
HGVS: NM_020223.4(FAM20C):c.646G>A (p.Gly216Arg)
Allele change: Missense_G216R

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.