Variant (rsID / SNP)

rs115019972

rs115019972 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH14. Location: chromosome 19, position 50,783,605. Clinical significance in the table: Benign.

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Reference-table entries

MYH14Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:50783605
Cytoband: 19q13.33
HGVS: NM_001145809.2(MYH14):c.4255C>T (p.Arg1419Trp)
Allele change: Missense_R1419W

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.