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Variant (rsID / SNP)

rs7543148

FMOD

rs7543148 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMOD. Location: chromosome 1, position 203,317,162. The table records no clinical significance for this variant.

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Reference-table entries

FMODNot classified
Variant type
synonymous_variant
Chromosome / position
1:203317162
HGVS
NM_002023.5,c.237G>A,p.Glu79Glu
Allele change
Synonymous_E79E

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.