List of variants in gene combination HBB, LOC106099062, LOC107133510, LOC110006319 studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.315+1G>A	rs33945777	0.00003
NM_000518.5(HBB):c.309C>A (p.Asn103Lys)	rs34227486	0.00001
NM_000518.4(HBB):c.308A>C (p.Asn103Thr)	rs33948057
NM_000518.5(HBB):c.307A>G (p.Asn103Asp)	rs33927739
NM_000518.5(HBB):c.314G>C (p.Arg105Thr)	rs33911434
NM_000518.5(HBB):c.315+3G>C	rs754412212
NM_000518.5(HBB):c.315+5G>A
NM_000518.5(HBB):c.315G>A (p.Arg105=)
NM_000518.5(HBB):c.315G>C (p.Arg105Ser)	rs33914944
NM_000518.5(HBB):c.315G>T (p.Arg105Ser)	rs33914944

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