List of variants in gene HBB, LOC106099062, LOC107133510 studied for Beta thalassemia intermedia

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.-137C>A	rs33941377	0.00004
NM_000518.5(HBB):c.-140C>T	rs34999973	0.00004
NC_000011.10:g.5227158G>A	rs33941377
NM_000518.4(HBB):c.-77_-76delAA	rs63750953
NM_000518.5(HBB):c.-137C>G	rs33941377
NM_000518.5(HBB):c.-142C>T	rs34883338
NM_000518.5(HBB):c.-81A>G	rs33981098
NM_000518.5(HBB):c.93-3T>G	rs34527846

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