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rs1064792986

From SNPedia

ClinVar
Risk rs1064792986(-;-)
Alt rs1064792986(-;-)
Reference Rs1064792986(GGCAAACACGGCCAGC;GGCAAACACGGCCAGC)
Significance Probable-Pathogenic
Disease Spastic paraplegia 31
Variation info
Gene REEP1
CLNDBN Spastic paraplegia 31, autosomal dominant
Reversed 1
HGVS NC_000002.11:g.86459790_86459805del16
CLNSRC
CLNACC RCV000460326.1,