rs4709746

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
rs4709746 has 4 RGD Records - Homo sapiens

  
Variant Page Assembly Chr Position Type Reference Nucleotide Variant Nucleotide Location Name Is Damaging? Visualize
1. View more GRCh38 6 163,711,969 - 163,711,970 snv C T - -
2. View more GRCh38 6 163,711,969 - 163,711,970 snv C T - -
3. View more GRCh38 6 163,711,969 - 163,711,970 snv C ? - -
4. View more GRCh38 6 163,711,969 - 163,711,970 snv C C - -