List of variants in gene OR9A4 reported as uncertain significance by Ambry Genetics

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001001656.3(OR9A4):c.169C>G (p.Pro57Ala)	rs200119127	0.00052
NM_001001656.3(OR9A4):c.329C>T (p.Thr110Ile)	rs200060570	0.00004
NM_001001656.3(OR9A4):c.187G>A (p.Gly63Ser)	rs568549409	0.00003
NM_001001656.3(OR9A4):c.700C>G (p.Arg234Gly)	rs782695340	0.00003
NM_001001656.3(OR9A4):c.276A>G (p.Ile92Met)	rs2485503984	0.00001
NM_001001656.3(OR9A4):c.452T>C (p.Phe151Ser)	rs1802240456	0.00001
NM_001001656.3(OR9A4):c.613T>C (p.Phe205Leu)	rs781849322	0.00001
NM_001001656.3(OR9A4):c.889G>A (p.Val297Ile)	rs781973881	0.00001
NM_001001656.3(OR9A4):c.116T>C (p.Met39Thr)
NM_001001656.3(OR9A4):c.173T>A (p.Met58Lys)
NM_001001656.3(OR9A4):c.247G>A (p.Gly83Arg)
NM_001001656.3(OR9A4):c.278A>G (p.Tyr93Cys)	rs782101774
NM_001001656.3(OR9A4):c.278A>T (p.Tyr93Phe)	rs782101774
NM_001001656.3(OR9A4):c.373G>A (p.Ala125Thr)	rs1802237988
NM_001001656.3(OR9A4):c.377T>G (p.Val126Gly)
NM_001001656.3(OR9A4):c.400A>G (p.Ile134Val)
NM_001001656.3(OR9A4):c.542G>C (p.Arg181Pro)	rs782482254
NM_001001656.3(OR9A4):c.599T>A (p.Phe200Tyr)	rs2485504800
NM_001001656.3(OR9A4):c.628T>C (p.Ser210Pro)
NM_001001656.3(OR9A4):c.673A>G (p.Ile225Val)	rs2485504993
NM_001001656.3(OR9A4):c.718A>G (p.Thr240Ala)
NM_001001656.3(OR9A4):c.727T>C (p.Ser243Pro)	rs374422987
NM_001001656.3(OR9A4):c.727T>G (p.Ser243Ala)	rs374422987
NM_001001656.3(OR9A4):c.73A>T (p.Ile25Phe)
NM_001001656.3(OR9A4):c.788A>G (p.Lys263Arg)	rs556697772
NM_001001656.3(OR9A4):c.920G>T (p.Arg307Leu)	rs782633602
NM_001001656.3(OR9A4):c.939G>C (p.Arg313Ser)	rs2128958837

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