Variant (rsID / SNP)

rs199915414

rs199915414 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH14. Location: chromosome 19, position 50,794,261. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MYH14Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:50794261
Cytoband: 19q13.33
HGVS: NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg)
Allele change: Missense_G1695R

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.