Variant: rs3819817 

    present in Gene: HAL
    present in Chromosome: 12
    Position on Chromosome: 95984993
    Alleles of this Variant: C/T

rs3819817 in HAL gene and Vitamin D measurement PMID 28757204 2017 Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis.

rs3819817 in HAL gene and Vitamin D3 measurement PMID 28757204 2017 Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis.