List of variants in gene THBD reported as likely benign for immune system disorder

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000361.3(THBD):c.127G>A (p.Ala43Thr)	rs1800576	0.00255
NM_000361.3(THBD):c.1502C>T (p.Pro501Leu)	rs1800579	0.00193
NM_000361.3(THBD):c.*158G>A	rs3176121	0.00118
NM_000361.3(THBD):c.1208G>A (p.Arg403Lys)	rs41400249	0.00036
NM_000361.3(THBD):c.-12C>T	rs370548660	0.00026
NM_000361.3(THBD):c.*325T>C	rs186669520	0.00014
NM_000361.3(THBD):c.1083G>A (p.Glu361=)	rs370377519	0.00003
NM_000361.3(THBD):c.1517C>A (p.Thr506Asn)	rs572623850	0.00001
NM_000361.3(THBD):c.920C>T (p.Ser307Leu)	rs372556297	0.00001
NM_000361.3(THBD):c.1057C>A (p.Pro353Thr)

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