List of variants in gene SURF1 reported as benign by GeneDx

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: 19

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HGVS	dbSNP	gnomAD frequency
NC_000009.12:g.133351735=	rs484248	0.47130
NM_003172.4(SURF1):c.106+81G>C	rs59358281	0.28937
NM_003172.4(SURF1):c.833+27C>T	rs2021976	0.07984
NM_003172.4(SURF1):c.*118T>C	rs4962133	0.05734
NM_003172.4(SURF1):c.515+213A>G	rs34847665	0.05728
NM_003172.4(SURF1):c.515+276C>T	rs28483151	0.05728
NM_003172.4(SURF1):c.573C>G (p.Thr191=)	rs28715079	0.05492
NM_003172.4(SURF1):c.280T>C (p.Leu94=)	rs28615629	0.04975
NM_003172.4(SURF1):c.752-65A>T	rs183853102	0.03605
NM_003172.4(SURF1):c.106+250A>G	rs111324588	0.02010
NM_003172.4(SURF1):c.751+6T>C	rs41296099	0.01414
NM_003172.4(SURF1):c.167C>G (p.Ala56Gly)	rs116779216	0.01318
NM_003172.4(SURF1):c.543C>T (p.Phe181=)	rs62637580	0.01036
NM_003172.4(SURF1):c.604G>C (p.Asp202His)	rs72619327	0.00517
NM_003172.4(SURF1):c.883C>T (p.Arg295Cys)	rs147312193	0.00385
NM_003172.4(SURF1):c.834-13T>C	rs139870012	0.00318
NM_003172.4(SURF1):c.240+9C>T	rs376459836	0.00009
NC_000009.12:g.133351736=
NM_003172.2(SURF1):c.-37C>T	rs523304

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