ClinVar Miner

List of variants studied for hypertensive disorder by New York Genome Center

Included ClinVar conditions (60):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
GRCh38/hg38 10q11.22-11.23(chr10:45795500-50134000)
NM_001127217.3(SMAD9):c.281G>C (p.Arg94Pro) rs748334459
NM_001753.5(CAV1):c.257A>G (p.Lys86Arg)
NM_001753.5(CAV1):c.30G>C (p.Glu10Asp) rs2115921451
NM_001753.5(CAV1):c.326T>A (p.Ile109Asn)

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