ClinVar Miner

List of variants studied for chromosome 10 disorder by GenomeConnect - Brain Gene Registry

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_016628.5(WAC):c.-3T>C rs2132290252
NM_016628.5(WAC):c.1101dup (p.Pro368fs) rs1841061596
NM_016628.5(WAC):c.1424C>G (p.Ser475Ter) rs2132834581
NM_016628.5(WAC):c.78+1G>A rs2132295469

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