List of variants in gene WDR62 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 37

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HGVS	dbSNP	gnomAD frequency
NM_001083961.2(WDR62):c.2147-34G>A	rs2301736	0.41985
NM_001083961.2(WDR62):c.700-18C>T	rs10423651	0.28763
NM_001083961.2(WDR62):c.1643-39G>A	rs2301735	0.07203
NM_001083961.2(WDR62):c.1768+28G>A	rs77938609	0.04228
NM_001083961.2(WDR62):c.561+44C>G	rs115806759	0.03880
NM_001083961.2(WDR62):c.4153+37C>G	rs58041656	0.03299
NM_001083961.2(WDR62):c.3514+44G>A	rs45468494	0.03042
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu)	rs35811023	0.00416
NM_001083961.2(WDR62):c.3812C>T (p.Ala1271Val)	rs111294536	0.00310
NM_001083961.2(WDR62):c.4312-5T>G	rs182467995	0.00215
NM_001083961.2(WDR62):c.4338C>T (p.Thr1446=)	rs149289227	0.00183
NM_001083961.2(WDR62):c.3786C>T (p.Gly1262=)	rs148415080	0.00176
NM_001083961.2(WDR62):c.2016C>T (p.Asp672=)	rs114968951	0.00170
NM_001083961.2(WDR62):c.3033G>A (p.Pro1011=)	rs118175551	0.00148
NM_001083961.2(WDR62):c.2211-4G>A	rs202109439	0.00096
NM_001083961.2(WDR62):c.3303G>A (p.Thr1101=)	rs117887683	0.00078
NM_001083961.2(WDR62):c.2529C>T (p.Asp843=)	rs144697999	0.00073
NM_001083961.2(WDR62):c.3612C>T (p.Gly1204=)	rs139946168	0.00066
NM_001083961.2(WDR62):c.4159C>A (p.Leu1387Ile)	rs147652186	0.00041
NM_001083961.2(WDR62):c.2976G>A (p.Ser992=)	rs757294519	0.00035
NM_001083961.2(WDR62):c.4312T>A (p.Leu1438Met)	rs138814793	0.00019
NM_001083961.2(WDR62):c.390+7C>T	rs759572399	0.00016
NM_001083961.2(WDR62):c.2766C>T (p.Arg922=)	rs373906889	0.00013
NM_001083961.2(WDR62):c.4527G>A (p.Ser1509=)	rs374574870	0.00006
NM_001083961.2(WDR62):c.1434C>G (p.Phe478Leu)	rs542178534	0.00001
NM_001083961.2(WDR62):c.2805T>A (p.Ser935=)	rs760951651	0.00001
NM_001083961.2(WDR62):c.2982G>A (p.Glu994=)	rs587784551	0.00001
NM_001083961.2(WDR62):c.4473G>A (p.Pro1491=)	rs757729585	0.00001
NM_001083961.2(WDR62):c.4501C>T (p.Leu1501=)	rs1204833868	0.00001
NM_001083961.2(WDR62):c.1233+15del	rs373693641
NM_001083961.2(WDR62):c.2112G>C (p.Ser704=)	rs115453534
NM_001083961.2(WDR62):c.2334-29C>T	rs2301737
NM_001083961.2(WDR62):c.3954C>T (p.Gly1318=)	rs773442664
NM_001083961.2(WDR62):c.4158A>C (p.Ala1386=)	rs1470780343
NM_001083961.2(WDR62):c.423T>C (p.Asp141=)	rs1174425209
NM_001083961.2(WDR62):c.540G>A (p.Val180=)	rs1555712171
NM_001083961.2(WDR62):c.831C>T (p.Leu277=)	rs549410799

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