List of variants in gene RTTN reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_173630.4(RTTN):c.5212C>T (p.His1738Tyr)	rs35068710	0.00210
NM_173630.4(RTTN):c.2804A>G (p.His935Arg)	rs145832674	0.00164
NM_173630.4(RTTN):c.2568T>A (p.Ala856=)	rs370998068	0.00061
NM_173630.4(RTTN):c.6080C>T (p.Thr2027Met)	rs199546509	0.00025
NM_173630.4(RTTN):c.1738C>T (p.Arg580Cys)	rs368918234	0.00014
NM_173630.4(RTTN):c.5055A>G (p.Leu1685=)	rs372431222	0.00014
NM_173630.4(RTTN):c.4234G>A (p.Gly1412Ser)	rs370765246	0.00006
NM_173630.4(RTTN):c.4877C>T (p.Thr1626Met)	rs781683199	0.00006
NM_173630.4(RTTN):c.3401C>G (p.Pro1134Arg)	rs751565369	0.00005
NM_173630.4(RTTN):c.1869G>T (p.Leu623Phe)	rs757634334	0.00002
NM_173630.4(RTTN):c.6443C>A (p.Ala2148Asp)	rs757807524	0.00001
NM_173630.4(RTTN):c.2203A>G (p.Asn735Asp)	rs2060468580
NM_173630.4(RTTN):c.4374G>A (p.Gln1458=)	rs1459805081
NM_173630.4(RTTN):c.4856G>A (p.Ser1619Asn)	rs1599327363
NM_173630.4(RTTN):c.5049A>T (p.Glu1683Asp)	rs1599300112
NM_173630.4(RTTN):c.6125C>T (p.Ser2042Leu)

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