ClinVar Miner

List of variants reported as benign for Fabry disease by Color

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_000169.2(GLA):c.-10C>T rs2071225
NM_000169.2(GLA):c.-12G>A rs3027585
NM_000169.2(GLA):c.1153A>G (p.Thr385Ala) rs397515869
NM_000169.2(GLA):c.129C>T (p.Gly43=) rs146177035
NM_000169.2(GLA):c.937G>T (p.Asp313Tyr) rs28935490

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