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rs137853869

From SNPedia

ClinVar
Risk rs137853869(;)
Alt rs137853869(;)
Reference rs137853869(AAGA;AAGA)
Significance Pathogenic
Disease Osteogenesis imperfecta type 9 not provided
Variation info
Gene PPIB SNX22
CLNDBN Osteogenesis imperfecta type 9 not provided
Reversed 1
HGVS NC_000015.9:g.64448314_64448317delTCTT
CLNSRC OMIM Allelic Variant Osteogenesis Imperfecta Variant Database (PPIB)
CLNACC RCV000018433.27, RCV000024535.1,