about
An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a BioGenoMEL study.Association of FTO Gene Variant (rs8050136) with Type 2 Diabetes and Markers of Obesity, Glycaemic Control and InflammationApplication of targeted panel sequencing and whole exome sequencing for 76 Chinese families with retinitis pigmentosa
P921
Q28371632-DD76E46E-0C7F-4530-81F6-3CBA1BC5213DQ28444945-A2FFCE7E-661B-4F01-8B65-32C938CFC0C5Q28444948-A9972B96-AC49-4244-89A8-DB81DC8D8E27Q28444960-84FA3961-663F-4A1D-A46D-4FD214D72311Q28444961-B68064CF-3D34-4C4A-87E4-08FAF7AAD58AQ28444979-3B2F3E49-D7BD-4220-A1CD-E9BBF5DDEBD3Q28445012-F94ED09F-2615-4F2B-9DEB-5FC27F849B8EQ28445087-101AD13F-0B9B-4FD0-BE90-C2D04DB6234BQ28445138-4D934844-6017-48BA-954A-92C472AB266DQ28445167-C0847D0A-2ACE-4F83-AE5C-75F857027974Q28445230-46B83E05-04CC-4E24-BBF3-C6FE3BB5C54AQ28546502-CAD2FDF5-C348-4871-BCB5-DB7D7AC6995A
P31
description
A sequence variant where the structure of the gene is changed.
@en
name
Gene Variant
@en
type
label
Gene Variant
@en
prefLabel
Gene Variant
@en
P279
P3986
SO:0001564