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Variant (rsID / SNP)

rs174535

MYRF

rs174535 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYRF. Location: chromosome 11, position 61,551,356. The table records no clinical significance for this variant.

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Reference-table entries

MYRFNot classified
Variant type
synonymous_variant
Chromosome / position
11:61551356
HGVS
NM_001127392.3,c.3153T>C,p.Ser1051Ser
Allele change
Synonymous_S1051S

Associated conditions / phenotypes

Colorectal Adenoma|Colorectal Cancer|Adenoma|Fetal Akinesia Deformation Sequence 2|Fetal Akinesia Deformation Sequence 3

Public references

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