Variants in gene FRAS1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_025074.7(FRAS1):c.11717T>C (p.Ile3906Thr)	rs61748814	0.01397
NM_025074.7(FRAS1):c.11907C>G (p.His3969Gln)	rs140492803	0.00272
NM_025074.7(FRAS1):c.11605A>G (p.Ile3869Val)	rs145035489	0.00236
NM_025074.7(FRAS1):c.10594A>G (p.Ile3532Val)	rs144715071	0.00232
NM_025074.7(FRAS1):c.7029+7G>A	rs183687186	0.00159
NM_025074.7(FRAS1):c.108+10T>G	rs76831011	0.00115
NM_025074.7(FRAS1):c.641C>T (p.Pro214Leu)	rs200053639	0.00108
NM_025074.7(FRAS1):c.9446C>T (p.Thr3149Met)	rs150680111	0.00080
NM_025074.7(FRAS1):c.9296G>A (p.Arg3099Gln)	rs149692526	0.00071
NM_025074.7(FRAS1):c.5725G>A (p.Val1909Ile)	rs182652779	0.00049
NM_025074.7(FRAS1):c.9627C>T (p.Tyr3209=)	rs377369857	0.00036
NM_025074.7(FRAS1):c.4181G>C (p.Gly1394Ala)	rs376487875	0.00010
NM_025074.7(FRAS1):c.39G>A (p.Ala13=)	rs773457837	0.00006

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