ClinVar Miner

List of variants in gene CDHR1 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_033100.4(CDHR1):c.*134C>T rs41291356
NM_033100.4(CDHR1):c.*1383dup rs147801078
NM_033100.4(CDHR1):c.*173C>A rs41291358
NM_033100.4(CDHR1):c.*2589G>A rs56127582
NM_033100.4(CDHR1):c.*342C>G rs7908492
NM_033100.4(CDHR1):c.*394G>A rs7907675
NM_033100.4(CDHR1):c.*503C>T rs7908753
NM_033100.4(CDHR1):c.*893C>T rs6585846
NM_033100.4(CDHR1):c.*907G>A rs12356218
NM_033100.4(CDHR1):c.1515C>T (p.Gly505=) rs116594644
NM_033100.4(CDHR1):c.2434C>T (p.Pro812Ser) rs45584033
NM_033100.4(CDHR1):c.297+6G>A rs79239487
NM_033100.4(CDHR1):c.486G>C (p.Arg162Ser) rs74145715
NM_033100.4(CDHR1):c.728C>T (p.Ala243Val) rs7086200
NM_033100.4(CDHR1):c.863-9C>T rs4933977

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