ClinVar Miner

List of variants in gene PTCH1 reported as likely benign by CSER _CC_NCGL, University of Washington

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000264.5(PTCH1):c.3155C>T (p.Thr1052Met) rs138911275 0.00066
NM_000264.5(PTCH1):c.3634G>A (p.Gly1212Ser) rs559827048 0.00003

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