rs6426749

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
rs6426749 has 3 RGD Records - Homo sapiens

  
Variant Page
Assembly
Chr
Position
Type
Reference Nucleotide
Variant Nucleotide
Location Name
Is Damaging?
Visualize
1. View more GRCh38 1 22,384,980 - 22,384,981 snv G C - -
2. View more GRCh38 1 22,384,980 - 22,384,981 snv G ? - -
3. View more GRCh38 1 22,384,980 - 22,384,981 snv G G - -