List of variants in gene combination BAG2, RAB23 reported as uncertain significance for congenital limb malformation

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_004282.4(BAG2):c.*5020C>T	rs182662	0.01805
NM_004282.4(BAG2):c.*4263C>T	rs549684091	0.00093
NM_004282.4(BAG2):c.*3685C>T	rs547766165	0.00079
NM_004282.4(BAG2):c.*5549A>G	rs143345846	0.00076
NM_004282.4(BAG2):c.*3238G>A	rs749068215	0.00029
NM_004282.4(BAG2):c.*3590C>T	rs773395495	0.00016
NM_004282.4(BAG2):c.*4737A>C	rs778774458	0.00016
NM_004282.4(BAG2):c.*5140G>C	rs541307925	0.00016
NM_004282.4(BAG2):c.*3518C>T	rs896219710	0.00014
NM_004282.4(BAG2):c.*3142C>G	rs562371430	0.00011
NM_004282.4(BAG2):c.*3395A>G	rs561133735	0.00011
NM_004282.4(BAG2):c.*3502G>T	rs550035886	0.00011
NM_004282.4(BAG2):c.*5351G>C	rs530900959	0.00011
NM_004282.4(BAG2):c.4604_4606dup	rs886061651	0.00006
NM_004282.4(BAG2):c.*3930G>T	rs571856902	0.00004
NM_004282.4(BAG2):c.*4204T>C	rs191147024	0.00004
NM_004282.4(BAG2):c.*3952A>G	rs1159890588	0.00001
NM_004282.4(BAG2):c.*4026A>G	rs908169983	0.00001
NM_004282.4(BAG2):c.*5476C>T	rs1387081917	0.00001
NM_004282.4(BAG2):c.*2973T>C	rs1170431413
NM_004282.4(BAG2):c.*4454T>C	rs368441472
NM_004282.4(BAG2):c.*4735A>C	rs931746824
NM_004282.4(BAG2):c.*4777T>C	rs1764724130
NM_004282.4(BAG2):c.*5084TGAT[3]	rs139778770
NM_004282.4(BAG2):c.*5219A>G	rs1764744688
NM_004282.4(BAG2):c.*5421T>C	rs1764753710
NM_004282.4(BAG2):c.*5536A>C	rs886061652

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