List of variants in gene MED25, MIR6800 studied for Charcot-Marie-Tooth disease type 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_030973.4(MED25):c.1316+19C>T	rs566927009	0.00004
NM_030973.4(MED25):c.1314C>G (p.Asn438Lys)	rs149030211	0.00002
NM_030973.4(MED25):c.1317-9C>T	rs370255278	0.00002
NM_030973.4(MED25):c.1317-3C>T	rs367774572	0.00001
NM_030973.4(MED25):c.1316+12T>C
NM_030973.4(MED25):c.1316+14_1316+15del
NM_030973.4(MED25):c.1316+18G>A
NM_030973.4(MED25):c.1316+1G>A
NM_030973.4(MED25):c.1316+20G>A
NM_030973.4(MED25):c.1316+20G>C	rs533964778
NM_030973.4(MED25):c.1316+23del
NM_030973.4(MED25):c.1316+8A>G
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.1317-3del	rs2074062033
NM_030973.4(MED25):c.1317-8G>A	rs1036590547
NM_030973.4(MED25):c.1317-8G>T	rs1036590547

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