ClinVar Miner

Variants with conflicting interpretations "association" and "likely risk allele"

Submission 1 (association) minimum review status:		Submission 1 (association) method:
Submission 2 (likely risk allele) minimum review status:		Submission 2 (likely risk allele) method:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.1574-3777G>T	rs2736100	0.52208
NM_001379610.1(SPINK1):c.101A>G (p.Asn34Ser)	rs17107315	0.00797

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