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Variant (rsID / SNP)

rs1057925

NFYC

rs1057925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NFYC. Location: chromosome 1, position 41,204,569. The table records no clinical significance for this variant.

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Reference-table entries

NFYCNot classified
Variant type
synonymous_variant
Chromosome / position
1:41204569
HGVS
NM_001308114.1,c.54C>T,p.Ser18Ser
Allele change
Synonymous_S18S

Associated conditions / phenotypes

Synonymous_S18S|Synonymous_S18S

Public references

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