Variant (rsID / SNP)

rs3756772

rs3756772 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FRK. Location: chromosome 6, position 116,325,142. The table records no clinical significance for this variant.

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Reference-table entries

FRKNot classified

Variant type: missense_variant
Chromosome / position: 6:116325142
HGVS: NM_002031.3,c.364G>A,p.Gly122Arg
Allele change: Missense_G122R

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.