PXDNL c.164+7218G>T

Variant ID: 8-52714523-C-A

NM_144651.4(PXDNL):c.164+7218G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage.

Human Molecular Genetics
Stanford, Janet L JL; FitzGerald, Liesel M LM; McDonnell, Shannon K SK; Carlson, Erin E EE; McIntosh, Laura M LM; Deutsch, Kerry K; Hood, Lee L; Ostrander, Elaine A EA; Schaid, Daniel J DJ
Publication Date: 2009-05-15

Variant appearance in text: rs718251
PubMed Link: 19251732
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.

American Journal Of Human Genetics
Suarez, Brian K BK; Duan, Jubao J; Sanders, Alan R AR; Hinrichs, Anthony L AL; Jin, Carol H CH; Hou, Cuiping C; Buccola, Nancy G NG; Hale, Nancy N; Weilbaecher, Ann N AN; Nertney, Deborah A DA; Olincy, Ann A; Green, Susan S; Schaffer, Arthur W AW; Smith, Christopher J CJ; Hannah, Dominique E DE; Rice, John P JP; Cox, Nancy J NJ; Martinez, Maria M; Mowry, Bryan J BJ; Amin, Farooq F; Silverman, Jeremy M JM; Black, Donald W DW; Byerley, William F WF; Crowe, Raymond R RR; Freedman, Robert R; Cloninger, C Robert CR; Levinson, Douglas F DF; Gejman, Pablo V PV
Publication Date: 2006-02

Variant appearance in text: rs718251
PubMed Link: 16400611
Variant Present in the following documents:
  • Main text
View BVdb publication page