ClinVar Miner

List of variants in gene GDNF reported as likely benign for Hirschsprung Disease, Dominant

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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_000514.4(GDNF):c.*1004T>C rs79370077
NM_000514.4(GDNF):c.*1141C>A rs2972929
NM_000514.4(GDNF):c.*1264C>T rs62360370
NM_000514.4(GDNF):c.*1276A>G rs142426358
NM_000514.4(GDNF):c.*131_*133GGA[10] rs150577324
NM_000514.4(GDNF):c.*1389A>G rs78613670
NM_000514.4(GDNF):c.*1541T>A rs138502514
NM_000514.4(GDNF):c.*1651A>G rs11111
NM_000514.4(GDNF):c.*1785G>T rs115322727
NM_000514.4(GDNF):c.*1898C>A rs547628776
NM_000514.4(GDNF):c.*2162G>T rs17379771
NM_000514.4(GDNF):c.*2204G>T rs72745194
NM_000514.4(GDNF):c.*2440G>A rs78865769
NM_000514.4(GDNF):c.*2643C>T rs146664109
NM_000514.4(GDNF):c.*2713G>A rs143311673
NM_000514.4(GDNF):c.*2883G>A rs77776214
NM_000514.4(GDNF):c.*363A>T rs45611434
NM_000514.4(GDNF):c.*529G>A rs58787312
NM_000514.4(GDNF):c.*93A>T rs45535335
NM_000514.4(GDNF):c.*988A>G rs79669773
NM_000514.4(GDNF):c.-227_-225CGG[6] rs554953764
NM_000514.4(GDNF):c.429G>A (p.Arg143=) rs36010631
NM_000514.4(GDNF):c.448G>A (p.Asp150Asn) rs76466003

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