List of variants in gene CACNA2D1 reported as likely benign for not specified

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000722.4(CACNA2D1):c.3134A>C (p.Asp1045Ala)	rs35131433	0.00374
NM_000722.4(CACNA2D1):c.659-19C>T	rs200166451	0.00353
NM_000722.4(CACNA2D1):c.-40C>G	rs200428602	0.00138
NM_000722.4(CACNA2D1):c.1735-6T>C	rs111772206	0.00084
NM_000722.4(CACNA2D1):c.2463+13T>A	rs771850068	0.00034
NM_000722.4(CACNA2D1):c.659-15T>A	rs1046985886	0.00031
NM_000722.4(CACNA2D1):c.1273-12T>C	rs560674806	0.00026
NM_000722.4(CACNA2D1):c.1516-14T>C	rs375141743	0.00024
NM_000722.4(CACNA2D1):c.1735-17G>A	rs367841992	0.00019
NM_000722.4(CACNA2D1):c.728+13A>C	rs149406906	0.00012
NM_000722.4(CACNA2D1):c.528A>C (p.Ser176=)	rs138577227	0.00009
NM_000722.4(CACNA2D1):c.1740T>C (p.Tyr580=)	rs761279886	0.00005
NM_000722.4(CACNA2D1):c.2967-15A>G	rs750119271	0.00005
NM_000722.4(CACNA2D1):c.1158G>A (p.Thr386=)	rs753918568	0.00004
NM_000722.4(CACNA2D1):c.1441-12C>G	rs559623642	0.00004
NM_000722.4(CACNA2D1):c.1796+8A>G	rs200882576	0.00004
NM_000722.4(CACNA2D1):c.2054-20A>G	rs751143429	0.00004
NM_000722.4(CACNA2D1):c.1611A>G (p.Pro537=)	rs76594260	0.00003
NM_000722.4(CACNA2D1):c.2682C>T (p.Pro894=)	rs147728344	0.00002
NM_000722.4(CACNA2D1):c.2869C>T (p.Leu957=)	rs767963200	0.00002
NM_000722.4(CACNA2D1):c.-40C>T	rs200428602
NM_000722.4(CACNA2D1):c.1590+19T>C	rs1554348402
NM_000722.4(CACNA2D1):c.1662+15T>C	rs1554345032
NM_000722.4(CACNA2D1):c.1873+14A>T	rs1057524018
NM_000722.4(CACNA2D1):c.2085T>C (p.Leu695=)	rs1554333976
NM_000722.4(CACNA2D1):c.2727+8del	rs538712996
NM_000722.4(CACNA2D1):c.3160-19_3160-15del	rs778907208

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