List of variants in gene CYP24A1 reported as likely benign for Hypercalcemia, infantile, 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000782.5(CYP24A1):c.234T>G (p.Gly78=)	rs61755338	0.01605
NM_000782.5(CYP24A1):c.470G>A (p.Arg157Gln)	rs35051736	0.00377
NM_000782.5(CYP24A1):c.604G>C (p.Asp202His)	rs114579367	0.00192
NM_000782.5(CYP24A1):c.616G>A (p.Glu206Lys)	rs115260488	0.00065
NM_000782.5(CYP24A1):c.378G>A (p.Pro126=)	rs116104487	0.00062
NM_000782.5(CYP24A1):c.93G>A (p.Thr31=)	rs151204685	0.00022
NM_000782.5(CYP24A1):c.753G>A (p.Arg251=)	rs377533549	0.00011
NM_000782.5(CYP24A1):c.150C>T (p.Gly50=)	rs566481776	0.00009
NM_000782.5(CYP24A1):c.733-9T>C	rs895309596	0.00009
NM_000782.5(CYP24A1):c.1083T>C (p.Pro361=)	rs147886742	0.00006
NM_000782.5(CYP24A1):c.1020C>T (p.Tyr340=)	rs77764129	0.00004
NM_000782.5(CYP24A1):c.439C>T (p.Leu147=)	rs774042537	0.00003
NM_000782.5(CYP24A1):c.172C>T (p.Leu58=)	rs761949738	0.00001
NM_000782.5(CYP24A1):c.577C>A (p.Leu193Ile)	rs377696502	0.00001
NM_000782.5(CYP24A1):c.114G>T (p.Pro38=)	rs61749689
NM_000782.5(CYP24A1):c.469C>A (p.Arg157=)	rs35873579

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