Variant (rsID / SNP)
rs1422795
rs1422795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAM19. Location: chromosome 5, position 156,936,364. The table records no clinical significance for this variant.
Reference-table entries
ADAM19Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:156936364
- HGVS
- NM_033274.5,c.850A>G,p.Ser284Gly
- Allele change
- Missense_S284G
Associated conditions / phenotypes
Aging|Major Affective Disorder 8|Type 2 Diabetes Mellitus|Major Affective Disorder 9|Diabetes Mellitus|Lung Disease|Bipolar Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.