List of variants reported as likely benign for amyloidosis by Labcorp Genetics (formerly Invitae), Labcorp

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 92

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.190T>C (p.Phe64Leu)	rs138065384	0.00019
NM_000371.4(TTR):c.384C>T (p.Ala128=)	rs143906738	0.00015
NM_000371.4(TTR):c.354C>T (p.Asn118=)	rs11541797	0.00009
NM_000371.4(TTR):c.411C>T (p.Ser137=)	rs759874627	0.00006
NM_000371.4(TTR):c.336+18C>T	rs370628373	0.00005
NM_000371.4(TTR):c.437A>G (p.Lys146Arg)	rs536294863	0.00005
NM_000371.4(TTR):c.375C>T (p.Tyr125=)	rs749079577	0.00004
NM_000371.4(TTR):c.267C>T (p.Tyr89=)	rs757950308	0.00003
NM_000371.4(TTR):c.405C>G (p.Ser135=)	rs760153126	0.00003
NM_000371.4(TTR):c.70-20C>T	rs773578107	0.00003
NM_000371.4(TTR):c.70-9T>C	rs764059061	0.00003
NM_000371.4(TTR):c.441A>G (p.Glu147=)	rs370056601	0.00002
NM_000371.4(TTR):c.78T>C (p.Gly26=)	rs779457244	0.00002
NM_000371.4(TTR):c.121C>A (p.Arg41=)	rs1004021945	0.00001
NM_000371.4(TTR):c.147C>T (p.Ala49=)	rs11081703	0.00001
NM_000371.4(TTR):c.200+15A>G	rs1485205541	0.00001
NM_000371.4(TTR):c.200+17C>A	rs767333203	0.00001
NM_000371.4(TTR):c.200+20T>C	rs2073494875	0.00001
NM_000371.4(TTR):c.201-16C>T	rs941725460	0.00001
NM_000371.4(TTR):c.24C>T (p.Leu8=)	rs991342939	0.00001
NM_000371.4(TTR):c.315C>A (p.Ser105=)	rs11541787	0.00001
NM_000371.4(TTR):c.336+8T>C	rs1176464590	0.00001
NM_000371.4(TTR):c.337-13T>C	rs762691667	0.00001
NM_000371.4(TTR):c.408T>C (p.Tyr136=)	rs1454790119	0.00001
NM_000371.4(TTR):c.40C>T (p.Leu14=)	rs1347695561	0.00001
NM_000371.4(TTR):c.69+12T>C	rs368643414	0.00001
NM_000371.4(TTR):c.70-16T>C	rs759512847	0.00001
NM_000371.4(TTR):c.75C>T (p.Thr25=)	rs750051388	0.00001
NM_000371.4(TTR):c.108T>A (p.Val36=)
NM_000371.4(TTR):c.114T>C (p.Asp38=)	rs779619795
NM_000371.4(TTR):c.117T>A (p.Ala39=)
NM_000371.4(TTR):c.120C>T (p.Val40=)
NM_000371.4(TTR):c.141T>C (p.Asn47=)	rs1252826226
NM_000371.4(TTR):c.147C>A (p.Ala49=)
NM_000371.4(TTR):c.156G>A (p.Val52=)	rs2144406775
NM_000371.4(TTR):c.160A>C (p.Arg54=)
NM_000371.4(TTR):c.174T>C (p.Asp58=)
NM_000371.4(TTR):c.180C>T (p.Thr60=)
NM_000371.4(TTR):c.186G>A (p.Glu62=)
NM_000371.4(TTR):c.195C>T (p.Ala65=)	rs571695233
NM_000371.4(TTR):c.198T>G (p.Ser66=)
NM_000371.4(TTR):c.200+12A>G
NM_000371.4(TTR):c.200+14G>T	rs2144406929
NM_000371.4(TTR):c.200+7del
NM_000371.4(TTR):c.200+8G>T	rs761675505
NM_000371.4(TTR):c.201-10C>A
NM_000371.4(TTR):c.201-10C>T	rs1380934184
NM_000371.4(TTR):c.201-16C>G
NM_000371.4(TTR):c.201-4A>G
NM_000371.4(TTR):c.201-7C>T
NM_000371.4(TTR):c.201-9A>C
NM_000371.4(TTR):c.216T>C (p.Ser72=)
NM_000371.4(TTR):c.21C>T (p.Leu7=)	rs2144405313
NM_000371.4(TTR):c.223C>T (p.Leu75=)	rs2073510448
NM_000371.4(TTR):c.231G>A (p.Gly77=)	rs1555631396
NM_000371.4(TTR):c.249A>G (p.Glu83=)
NM_000371.4(TTR):c.285C>T (p.Thr95=)
NM_000371.4(TTR):c.300G>A (p.Lys100=)	rs2144409644
NM_000371.4(TTR):c.327G>A (p.Glu109=)	rs876661395
NM_000371.4(TTR):c.330T>C (p.His110=)
NM_000371.4(TTR):c.333A>G (p.Ala111=)
NM_000371.4(TTR):c.336+10C>G
NM_000371.4(TTR):c.336+10C>T
NM_000371.4(TTR):c.337-12C>T
NM_000371.4(TTR):c.337-16C>G
NM_000371.4(TTR):c.337-19T>C
NM_000371.4(TTR):c.36T>C (p.Ala12=)
NM_000371.4(TTR):c.381T>C (p.Ile127=)
NM_000371.4(TTR):c.387C>A (p.Ala129=)
NM_000371.4(TTR):c.390G>A (p.Leu130=)
NM_000371.4(TTR):c.390G>C (p.Leu130=)
NM_000371.4(TTR):c.390G>T (p.Leu130=)
NM_000371.4(TTR):c.391C>T (p.Leu131=)	rs121918073
NM_000371.4(TTR):c.396C>T (p.Ser132=)	rs2144414307
NM_000371.4(TTR):c.423C>T (p.Val141=)	rs557320637
NM_000371.4(TTR):c.45A>G (p.Val15=)
NM_000371.4(TTR):c.54T>C (p.Ser18=)
NM_000371.4(TTR):c.57G>A (p.Glu19=)
NM_000371.4(TTR):c.66T>C (p.Pro22=)	rs2144405395
NM_000371.4(TTR):c.69+10T>C	rs1179187406
NM_000371.4(TTR):c.69+10del
NM_000371.4(TTR):c.69+13G>C	rs2073488528
NM_000371.4(TTR):c.69+7G>A	rs1453023289
NM_000371.4(TTR):c.6T>G (p.Ala2=)
NM_000371.4(TTR):c.70-19G>A	rs548935944
NM_000371.4(TTR):c.70-19G>C
NM_000371.4(TTR):c.70-19G>T	rs548935944
NM_000371.4(TTR):c.70-4C>T
NM_000371.4(TTR):c.70-5C>T	rs757103675
NM_000371.4(TTR):c.70-9T>A
NM_000371.4(TTR):c.72C>T (p.Gly24=)
NM_000371.4(TTR):c.9T>C (p.Ser3=)	rs1598843600

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