List of variants in gene SIX3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005413.4(SIX3):c.525G>A (p.Gln175=)	rs116680477	0.00907
NM_005413.4(SIX3):c.109G>T (p.Gly37Cys)	rs199823175	0.00210
NM_005413.4(SIX3):c.720G>T (p.Ala240=)	rs191012035	0.00185
NM_005413.4(SIX3):c.96C>T (p.Ser32=)	rs202214767	0.00042
NM_005413.4(SIX3):c.831G>A (p.Pro277=)	rs370941478	0.00022
NM_005413.4(SIX3):c.830C>A (p.Pro277Gln)	rs575632344	0.00007
NM_005413.4(SIX3):c.187GGC[6] (p.Gly69del)
NM_005413.4(SIX3):c.244C>T (p.Leu82=)
NM_005413.4(SIX3):c.831G>C (p.Pro277=)	rs370941478
NM_005413.4(SIX3):c.993T>C (p.Asp331=)
NM_005413.4(SIX3):c.99C>T (p.Gly33=)

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