ClinVar Miner

List of variants in gene LOC126860809, WDR37 studied for neurooculocardiogenitourinary syndrome

Included ClinVar conditions (1):

Neurooculocardiogenitourinary syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_014023.4(WDR37):c.726+22T>C	rs10794716	0.99093
NM_014023.4(WDR37):c.659A>G (p.Asp220Gly)	rs2131646026

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