ClinVar Miner

List of variants in gene combination MED25, MIR6800 reported as likely benign for peripheral neuropathy

Included ClinVar conditions (524):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_030973.4(MED25):c.1316+19C>T rs566927009 0.00004
NM_030973.4(MED25):c.1317-9C>T rs370255278 0.00002
NM_030973.4(MED25):c.1316+12T>C
NM_030973.4(MED25):c.1316+14_1316+15del
NM_030973.4(MED25):c.1316+20G>A
NM_030973.4(MED25):c.1316+20G>C rs533964778
NM_030973.4(MED25):c.1317-16del rs748829394
NM_030973.4(MED25):c.1317-19C>T
NM_030973.4(MED25):c.1317-20T>C
NM_030973.4(MED25):c.1317-8G>A rs1036590547
NM_030973.4(MED25):c.1317-8G>T rs1036590547

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