ClinVar Miner

List of variants in gene MBD5 reported as benign for not provided

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Gene type:
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Total variants: 26
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HGVS dbSNP
GRCh37/hg19 2q23.1(chr2:148808568-148812188)x1
GRCh37/hg19 2q23.1(chr2:148808568-148814430)x1
GRCh37/hg19 2q23.1(chr2:148814430-148861205)x1
GRCh37/hg19 2q23.1(chr2:148860592-148974600)x3
GRCh37/hg19 2q23.1(chr2:149065242-149069742)x1
GRCh37/hg19 2q23.1(chr2:149065395-149069742)x1
GRCh37/hg19 2q23.1(chr2:149109237-149178974)x1
GRCh37/hg19 2q23.1(chr2:149131384-149162368)x1
GRCh37/hg19 2q23.1(chr2:149170115-149202550)x1
GRCh37/hg19 2q23.1(chr2:149198831-149204775)x1
GRCh37/hg19 2q23.1(chr2:149199613-149202176)x1
GRCh37/hg19 2q23.1(chr2:149201266-149202550)x0
GRCh37/hg19 2q23.1(chr2:149204841-149244732)x3
GRCh37/hg19 2q23.1(chr2:149204841-149266085)x3
GRCh37/hg19 2q23.1(chr2:149206411-149239689)x3
GRCh37/hg19 2q23.1(chr2:149206411-149242773)x3
GRCh37/hg19 2q23.1(chr2:149206411-149244732)x3
GRCh37/hg19 2q23.1(chr2:149206821-149266085)x3
GRCh37/hg19 2q23.1(chr2:149248413-149250399)x1
NM_018328.4(MBD5):c.113+221A>G rs10928397
NM_018328.4(MBD5):c.156A>G (p.Thr52=) rs796958008
NM_018328.4(MBD5):c.1596A>G (p.Val532=) rs114611333
NM_018328.4(MBD5):c.4263+250A>C rs7574808
NM_018328.4(MBD5):c.4264-56G>A rs73003524
NM_018328.4(MBD5):c.4264-57C>T rs80229097
NM_018328.4(MBD5):c.4338-198dup rs151097491

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