List of variants in gene OBSL1 reported as benign by Illumina Laboratory Services, Illumina

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: 46

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HGVS	dbSNP	gnomAD frequency
NM_015311.3(OBSL1):c.4836A>G (p.Thr1612=)	rs10932813	0.98738
NM_015311.3(OBSL1):c.4395T>C (p.Asp1465=)	rs10932816	0.96819
NM_015311.3(OBSL1):c.4733A>G (p.Gln1578Arg)	rs10932814	0.96074
NM_015311.3(OBSL1):c.2168G>A (p.Arg723Lys)	rs1039898	0.81697
NM_015311.3(OBSL1):c.921T>C (p.Leu307=)	rs10180675	0.80936
NM_015311.3(OBSL1):c.4095G>C (p.Glu1365Asp)	rs1983210	0.69535
NM_015311.3(OBSL1):c.3561T>C (p.Pro1187=)	rs2278201	0.47513
NM_015311.3(OBSL1):c.5309-4C>G	rs34490902	0.45189
NM_015311.3(OBSL1):c.5300G>A (p.Arg1767Gln)	rs59332477	0.43789
NM_015311.3(OBSL1):c.580C>T (p.Leu194=)	rs1061399	0.35689
NM_015311.3(OBSL1):c.4566C>T (p.Cys1522=)	rs3087971	0.26702
NM_015311.3(OBSL1):c.2682C>T (p.Asp894=)	rs3183099	0.20573
NM_015311.3(OBSL1):c.2055C>A (p.Ala685=)	rs1043537	0.18910
NM_015311.3(OBSL1):c.1818C>T (p.Phe606=)	rs61732787	0.18850
NM_015311.3(OBSL1):c.1102C>T (p.Arg368Cys)	rs35009641	0.03933
NM_015311.3(OBSL1):c.-42T>C	rs879691022	0.01980
NM_015311.3(OBSL1):c.4117G>A (p.Glu1373Lys)	rs140214067	0.01955
NM_015311.3(OBSL1):c.4032C>G (p.Pro1344=)	rs112751766	0.01798
NM_015311.3(OBSL1):c.1884C>T (p.Tyr628=)	rs115194510	0.01551
NM_015311.3(OBSL1):c.3752C>T (p.Pro1251Leu)	rs145485683	0.01074
NM_015311.3(OBSL1):c.1512C>T (p.Thr504=)	rs138262993	0.00857
NM_015311.3(OBSL1):c.5202C>A (p.Asp1734Glu)	rs181520135	0.00757
NM_015311.3(OBSL1):c.3649G>A (p.Glu1217Lys)	rs72957510	0.00742
NM_015311.3(OBSL1):c.3950T>A (p.Leu1317Gln)	rs115283876	0.00740
NM_015311.3(OBSL1):c.4361G>A (p.Arg1454Gln)	rs183329050	0.00737
NM_015311.3(OBSL1):c.3003C>T (p.Ala1001=)	rs150691758	0.00634
NM_015311.3(OBSL1):c.4363T>C (p.Leu1455=)	rs78420199	0.00600
NM_015311.3(OBSL1):c.4192G>A (p.Val1398Ile)	rs147543583	0.00466
NM_015311.3(OBSL1):c.5280C>T (p.Pro1760=)	rs373081802	0.00398
NM_015311.3(OBSL1):c.3283G>A (p.Ala1095Thr)	rs186692362	0.00388
NM_015311.3(OBSL1):c.3399G>A (p.Gly1133=)	rs115915650	0.00387
NM_015311.3(OBSL1):c.1245G>A (p.Arg415=)	rs61732788	0.00371
NM_015311.3(OBSL1):c.4067-12C>T	rs144059707	0.00336
NM_015311.3(OBSL1):c.3390T>C (p.Gly1130=)	rs200777549	0.00327
NM_015311.3(OBSL1):c.375G>A (p.Glu125=)	rs374656370	0.00182
NM_015311.3(OBSL1):c.96G>A (p.Lys32=)	rs200451309	0.00108
NM_015311.3(OBSL1):c.2981G>A (p.Arg994His)	rs139713392	0.00054
NM_015311.3(OBSL1):c.2577G>T (p.Gly859=)	rs141559295	0.00052
NM_015311.3(OBSL1):c.2578C>T (p.Pro860Ser)	rs117788171	0.00052
NM_015311.3(OBSL1):c.1599G>A (p.Thr533=)	rs149009269	0.00029
NM_015311.3(OBSL1):c.3604G>A (p.Ala1202Thr)	rs201887372	0.00027
NM_015311.3(OBSL1):c.600G>A (p.Arg200=)	rs373739744	0.00001
NM_015311.3(OBSL1):c.-208G>C	rs567328066
NM_015311.3(OBSL1):c.-43del	rs747020402
NM_015311.3(OBSL1):c.2730C>A (p.Ala910=)	rs10804275
NM_015311.3(OBSL1):c.4067-11G>T	rs1983211

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