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rs797044852

From SNPedia

ClinVar
Risk rs797044852(;)
Alt rs797044852(;)
Reference rs797044852(TG;TG)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene FKBP10
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000017.10:g.39977285_39977286delTG
CLNSRC
CLNACC RCV000190651.1,