ClinVar Miner

List of variants in gene combination HOXA13, LOC107126288 reported as benign for hand-foot-genital syndrome

Included ClinVar conditions (2):

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_000522.5(HOXA13):c.496C>A (p.Pro166Thr)	rs34398255

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