ClinVar Miner

List of variants studied for hereditary peripheral neuropathy by NeuroMeGen, Hospital Clinico Santiago de Compostela

Included ClinVar conditions (479):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_024577.4(SH3TC2):c.2860C>T (p.Arg954Ter) rs80338933 0.00067
NM_002180.3(IGHMBP2):c.1327C>T (p.Arg443Cys) rs751549678 0.00001
NM_024577.4(SH3TC2):c.3511C>T (p.Arg1171Cys) rs759785462 0.00001
NM_000166.6(GJB1):c.547C>T (p.Arg183Cys) rs863224471
NM_001374736.1(DST):c.23402C>T (p.Pro7801Leu) rs1242078669
NM_001723.7(DST):c.5177dup (p.Thr1727fs) rs759006806
NM_002180.3(IGHMBP2):c.181G>A (p.Gly61Arg) rs1057518943
NM_007289.4(MME):c.1666C>T (p.Pro556Ser) rs1559961997
NM_007289.4(MME):c.1972G>A (p.Ala658Thr) rs1559963660
NM_018706.7(DHTKD1):c.1543C>A (p.Pro515Thr) rs762729182
NM_024577.4(SH3TC2):c.2640del (p.Asn881fs) rs1561764569

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