List of variants in gene FGFR2 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP
NM_022970.3(FGFR2):c.*1070T>C	rs886046761
NM_022970.3(FGFR2):c.*1126T>C	rs370106008
NM_022970.3(FGFR2):c.*1287A>C	rs886046760
NM_022970.3(FGFR2):c.*1369C>T	rs886046759
NM_022970.3(FGFR2):c.*1402T>C	rs886046758
NM_022970.3(FGFR2):c.*1489C>T	rs886046757
NM_022970.3(FGFR2):c.*497T>C	rs3135827
NM_022970.3(FGFR2):c.*674G>T	rs566155088
NM_022970.3(FGFR2):c.*736dup	rs886046762
NM_022970.3(FGFR2):c.-128G>A	rs547739869
NM_022970.3(FGFR2):c.-129C>T	rs886046765
NM_022970.3(FGFR2):c.-165G>A	rs886046766
NM_022970.3(FGFR2):c.-371C>T	rs527570655
NM_022970.3(FGFR2):c.-535G>C	rs886046767
NM_022970.3(FGFR2):c.-622G>A	rs886046768
NM_022970.3(FGFR2):c.110-22TC[3]	rs773932794
NM_022970.3(FGFR2):c.1182A>T (p.Val394=)	rs886046763
NM_022970.3(FGFR2):c.1542C>A (p.Thr514=)	rs74160617
NM_022970.3(FGFR2):c.1565-11A>G	rs41293744
NM_022970.3(FGFR2):c.204C>T (p.Ala68=)	rs747982371
NM_022970.3(FGFR2):c.2419G>A (p.Glu807Lys)	rs764959117
NM_022970.3(FGFR2):c.351T>C (p.Thr117=)	rs886046764

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