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rs786205638

From SNPedia

ClinVar
Risk rs786205638(;)
Alt rs786205638(;)
Reference rs786205638(TTAAAAGATACTTGAGCTGGGACACTCCTCAAGAAGTCATTGCAGTTA;TTAAAAGATACTTGAGCTGGGACACTCCTCAAGAAGTCATTGCAGTTA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DCAF17
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.172306382_172306429delTTAAAAGATACTTGAGCTGGGACACTCCTCAAGAAGTCATTGCAGTTA
CLNSRC
CLNACC RCV000171502.1,