rs2011614

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
rs2011614 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 17 30,454,774 - 30,454,775 snv G A INTRON -
2. View more GRCh38 17 30,454,774 - 30,454,775 snv G G INTRON -
3. View more GRCh38 17 30,454,774 - 30,454,775 snv G ? INTRON -