rs33945777[Variant ID] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 619686	NM_000518.5(HBB):c.315+1G>T	LOC107133510, LOC110006319 +2 more	Single nucleotide variant (splice donor variant)	not provided +1 more	GPathogenic
Select item 189128	NM_000518.5(HBB):c.315+1G>C	HBB, LOC106099062 +2 more	Single nucleotide variant (splice donor variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 15438	NM_000518.5(HBB):c.315+1G>A	LOC106099062, LOC107133510 +2 more	Single nucleotide variant (splice donor variant)	Beta-thalassemia HBB/LCRB +11 more	GPathogenic

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