ClinVar Miner

List of variants in gene GALC reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_000153.4(GALC):c.1033+145A>G rs17760463
NM_000153.4(GALC):c.1034-125G>C rs17760374
NM_000153.4(GALC):c.1034-270A>G rs78508589
NM_000153.4(GALC):c.1034-314A>G rs17687144
NM_000153.4(GALC):c.1072C>T (p.Leu358=) rs74073730
NM_000153.4(GALC):c.1161+301C>T rs3906822
NM_000153.4(GALC):c.1162-152G>A rs443019
NM_000153.4(GALC):c.1162-197T>C rs428542
NM_000153.4(GALC):c.1162-4del rs11300320
NM_000153.4(GALC):c.1252-115T>C rs440426
NM_000153.4(GALC):c.1252-166G>A rs451073
NM_000153.4(GALC):c.1302C>T (p.Ser434=) rs3213918
NM_000153.4(GALC):c.1338+159C>T rs3213917
NM_000153.4(GALC):c.1490-233C>T rs3910682
NM_000153.4(GALC):c.1670+204T>C rs430536
NM_000153.4(GALC):c.1670+94A>G rs444902
NM_000153.4(GALC):c.1671-319A>G rs367125
NM_000153.4(GALC):c.1911+122C>G rs45567441
NM_000153.4(GALC):c.1911+129G>A rs45626938
NM_000153.4(GALC):c.1912-170C>T rs433764
NM_000153.4(GALC):c.1912-220T>G rs390474
NM_000153.4(GALC):c.195+164G>A rs78727833
NM_000153.4(GALC):c.196-201del rs112118889
NM_000153.4(GALC):c.583-288G>A rs74563284
NM_000153.4(GALC):c.622-137CAAA[4] rs146880216
NM_000153.4(GALC):c.622-162del rs112016425
NM_000153.4(GALC):c.622-175C>T rs111931900
NM_000153.4(GALC):c.622-273G>A rs148708614
NM_000153.4(GALC):c.622-284C>T rs112469201
NM_000153.4(GALC):c.752+199A>T rs4904409
NM_000153.4(GALC):c.908+270T>A rs397644
NM_001201402.2(GALC):c.117+71T>C rs76999174

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