ClinVar Miner

List of variants reported as benign for cataract 4 multiple types

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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ClinVar version:
Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_006891.4(CRYGD):c.*12T>C rs2305429 0.92175
NM_006891.4(CRYGD):c.285A>G (p.Arg95=) rs2305430 0.87984
NM_006891.4(CRYGD):c.51T>C (p.Tyr17=) rs2242074 0.59825
NM_006891.4(CRYGD):c.130A>G (p.Met44Val) rs61731517 0.00834
NM_006891.4(CRYGD):c.252+7A>G rs185860020 0.00261
NM_006891.4(CRYGD):c.376G>A (p.Val126Met) rs150318966 0.00220
NM_006891.4(CRYGD):c.63C>T (p.Ser21=) rs150961505 0.00069
NM_006891.4(CRYGD):c.-39C>T rs765407471 0.00051
NM_006891.4(CRYGD):c.252+10T>A rs200111275 0.00031
NM_006891.4(CRYGD):c.10-7C>G rs189582567 0.00029
NM_006891.4(CRYGD):c.9+15C>T rs368318772 0.00014
NM_006891.4(CRYGD):c.-40C>T rs113618781 0.00013
NM_006891.4(CRYGD):c.499C>T (p.Leu167=) rs774626835 0.00011
NM_006891.4(CRYGD):c.189T>C (p.Tyr63=) rs200911604 0.00004
NM_006891.4(CRYGD):c.192C>G (p.Ala64=) rs766003243 0.00001
NM_006891.4(CRYGD):c.479C>T (p.Thr160Met) rs564197072 0.00001

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