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

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

Total variants with conflicting interpretations: 4

HGVS	dbSNP	gnomAD frequency
NM_001379610.1(SPINK1):c.101A>G (p.Asn34Ser)	rs17107315	0.00797
NM_007194.4(CHEK2):c.470T>C (p.Ile157Thr)	rs17879961	0.00408
NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met)	rs142763740	0.00032
NM_007194.4(CHEK2):c.1283C>T (p.Ser428Phe)	rs137853011	0.00026

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