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. Author manuscript; available in PMC: 2022 Apr 20.
Published in final edited form as: Mult Scler Relat Disord. 2021 Aug 2;55:103185. doi: 10.1016/j.msard.2021.103185

Fig. 4.

Fig. 4.

STK11 SNP prevalence

The C/T genotype % is shown for all groups. Significance (*, P<0.05) is indicated by black lines; near significance is indicated by gray lines. Data are taken from Table 2.