ClinVar Miner

List of variants in gene combination MBD5, ORC4

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_018328.5(MBD5):c.-974A>G rs1057521148 0.00003
GRCh37/hg19 2q22.3-23.1(chr2:148698523-148900148)
GRCh37/hg19 2q22.3-23.1(chr2:148698834-148954778)
GRCh37/hg19 2q23.1(chr2:148709803-148878665)x3
GRCh37/hg19 2q23.1(chr2:148710290-149021799)
GRCh37/hg19 2q23.1(chr2:148717346-148799306)x1
GRCh37/hg19 2q23.1(chr2:148724265-148861205)x1
GRCh37/hg19 2q23.1(chr2:148726315-148824342)x1
GRCh37/hg19 2q23.1(chr2:148728326-148851964)
GRCh37/hg19 2q23.1(chr2:148728409-149130479)
GRCh37/hg19 2q23.1(chr2:148746282-148802565)x1
GRCh37/hg19 2q23.1(chr2:148746282-148820654)x1
GRCh37/hg19 2q23.1(chr2:148746282-148897425)x1
GRCh37/hg19 2q23.1(chr2:148746282-149079105)
GRCh37/hg19 2q23.1(chr2:148755020-148862543)x1
GRCh37/hg19 2q23.1(chr2:148755020-149050963)x1
GRCh37/hg19 2q23.1(chr2:148762386-148932571)x1
GRCh37/hg19 2q23.1(chr2:148777298-148779627)x3
GRCh37/hg19 2q23.1(chr2:148777552-148991171)x1
GRCh37/hg19 2q23.1(chr2:148778595-148799306)x1
NC_000002.11:g.(?_148730288)_(149270510_?)del
NM_001378120.1(MBD5):c.-1112_-1111insGTT
NM_001378120.1(MBD5):c.-1114GCTACTGCTGCTGCT[1]
NM_001378120.1(MBD5):c.-1114GCTACTGCTGCTGCT[3]
NM_018328.5(MBD5):c.-962+16C>T rs1057520964
NM_018328.5(MBD5):c.-973G>A rs528390918

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