List of variants in gene TNFRSF13C reported as benign for hematologic 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_052945.4(TNFRSF13C):c.*120T>C	rs7290134	0.41881
NM_052945.4(TNFRSF13C):c.367+18G>A	rs200206184	0.00114
NM_052945.4(TNFRSF13C):c.368-15C>A	rs372331667	0.00073
NM_052945.4(TNFRSF13C):c.368-13C>G	rs201892760
NM_052945.4(TNFRSF13C):c.368-13C>T	rs201892760

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