Variant (rsID / SNP)

rs3795677

rs3795677 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMN2. Location: chromosome 1, position 240,492,734. The table records no clinical significance for this variant.

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Reference-table entries

FMN2Not classified

Variant type: missense_variant
Chromosome / position: 1:240492734
HGVS: NM_001305424.2,c.4415G>A,p.Arg1472His
Allele change: Missense_R775H

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.