Variant (rsID / SNP)

rs6952125

rs6952125 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM220A. Location: chromosome 7, position 6,370,194. The table records no clinical significance for this variant.

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Reference-table entries

FAM220ANot classified

Variant type: missense_variant
Chromosome / position: 7:6370194
HGVS: NM_001037163.2,c.592G>A,p.Val198Met
Allele change: Missense_V198M

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.