ClinVar Miner

List of variants in gene combination LOC130055403, TINF2 reported by Sema4, Sema4

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001099274.3(TINF2):c.74G>C (p.Gly25Ala)	rs202093758	0.00166
NM_001099274.3(TINF2):c.127G>A (p.Ala43Thr)	rs35653076	0.00014
NM_001099274.3(TINF2):c.146T>C (p.Val49Ala)	rs1594555802

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