Variant (rsID / SNP)
rs3900940
rs3900940 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH15. Location: chromosome 3, position 108,147,728. The table records no clinical significance for this variant.
Reference-table entries
MYH15Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 3:108147728
- HGVS
- NM_014981.3,c.3313A>G,p.Thr1105Ala
- Allele change
- Missense_T1125A
Associated conditions / phenotypes
Heart Disease|Coronary Heart Disease 1|Stroke, Ischemic
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.