List of variants in gene GDNF reported as benign for Hirschsprung disease 3

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 21

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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.*1199A>T
NM_000514.4(GDNF):c.*1264C>T	rs62360370
NM_000514.4(GDNF):c.*1389A>G	rs78613670
NM_000514.4(GDNF):c.*1541T>A	rs138502514
NM_000514.4(GDNF):c.*1605T>C	rs3749692
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.*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.*450C>T
NM_000514.4(GDNF):c.*529G>A	rs58787312
NM_000514.4(GDNF):c.-51A>G	rs2973033
NM_000514.4(GDNF):c.448G>A (p.Asp150Asn)	rs76466003
NM_000514.4(GDNF):c.540A>G (p.Arg180=)	rs112417561

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