LIPC c.88+6252T>C

Variant ID: 15-58730571-T-C

NM_000236.2(LIPC):c.88+6252T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.

Heredity
Shirali, M M; Pong-Wong, R R; Navarro, P P; Knott, S S; Hayward, C C; Vitart, V V; Rudan, I I; Campbell, H H; Hastie, N D ND; Wright, A F AF; Haley, C S CS
Publication Date: 2016-03

Variant appearance in text: rs6494006
PubMed Link: 26696135
Variant Present in the following documents:
  • Main text
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