List of variants in gene combination FGFR1, LOC102723716 reported as uncertain significance for Hypogonadotropic hypogonadism 2 with or without anosmia

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_023110.3(FGFR1):c.*1026T>C	rs542417198	0.00214
NM_023110.3(FGFR1):c.*1446A>C	rs578094209	0.00081
NM_023110.3(FGFR1):c.*1055C>T	rs761124911	0.00035
NM_023110.3(FGFR1):c.*2057C>T	rs556829066	0.00031
NM_023110.3(FGFR1):c.*2391A>G	rs185729862	0.00024
NM_023110.3(FGFR1):c.*1711G>A	rs567642271	0.00021
NM_023110.3(FGFR1):c.*2407C>T	rs758524862	0.00010
NM_023110.3(FGFR1):c.*957C>T	rs941835357	0.00009
NM_023110.3(FGFR1):c.*1286C>T	rs886062909	0.00003
NM_023110.3(FGFR1):c.*1560C>T	rs761096092	0.00003
NM_023110.3(FGFR1):c.*1965G>A	rs886062907	0.00003
NM_023110.3(FGFR1):c.*2408C>T	rs1004230937	0.00003
NM_023110.3(FGFR1):c.*762A>G	rs886062914	0.00003
NM_023110.3(FGFR1):c.*802C>T	rs938792635	0.00003
NM_023110.3(FGFR1):c.*991G>A	rs866647792	0.00003
NM_023110.3(FGFR1):c.*913G>A	rs886062912	0.00002
NM_023110.3(FGFR1):c.*1086A>T	rs1287148499	0.00001
NM_023110.3(FGFR1):c.*1149G>A	rs923197183	0.00001
NM_023110.3(FGFR1):c.*2445A>G	rs1261528641	0.00001
NM_023110.3(FGFR1):c.*928G>A	rs1814772534	0.00001
NM_023110.3(FGFR1):c.*1124C>G	rs561923573
NM_023110.3(FGFR1):c.*1144G>A	rs886062911
NM_023110.3(FGFR1):c.*1218T>C	rs886062910
NM_023110.3(FGFR1):c.*1616T>G	rs886062908
NM_023110.3(FGFR1):c.*1676G>A	rs763761019
NM_023110.3(FGFR1):c.*1723C>T	rs1200256665
NM_023110.3(FGFR1):c.*1823G>A	rs1814497706
NM_023110.3(FGFR1):c.*1982A>C	rs536000259
NM_023110.3(FGFR1):c.*819T>G	rs1814814648
NM_023110.3(FGFR1):c.*845T>C	rs886062913
NM_023110.3(FGFR1):c.*958G>A	rs537880800

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