List of variants in gene ABO reported as association

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_020469.3(ABO):c.29-4288A>G	rs2519093	0.83233
NM_020469.3(ABO):c.28+748T>C	rs532436	0.83181
NM_020469.3(ABO):c.28+1179T>C	rs507666	0.83172
NM_020469.2(ABO):c.[467C>T;803G>C]
NM_020469.3(ABO):c.28+867_28+868delinsA	rs1554760445

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