SLC45A2 c.888+919A>G

Variant ID: 5-33962877-T-C

NM_016180.3(SLC45A2):c.888+919A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Ancestry inference of 96 population samples using microhaplotypes.

International Journal Of Legal Medicine
Bulbul, Ozlem O; Pakstis, Andrew J AJ; Soundararajan, Usha U; Gurkan, Cemal C; Brissenden, Jane E JE; Roscoe, Janet M JM; Evsanaa, Baigalmaa B; Togtokh, Ariunaa A; Paschou, Peristera P; Grigorenko, Elena L EL; Gurwitz, David D; Wootton, Sharon S; Lagace, Robert R; Chang, Joseph J; Speed, William C WC; Kidd, Kenneth K KK
Publication Date: 2018-05

Variant appearance in text: rs1423676
PubMed Link: 29248957
Variant Present in the following documents:
  • Main text
  • 414_2017_Article_1748.pdf
View BVdb publication page