ClinVar Miner

List of variants studied for chromosome 10 disorder by Baylor Genetics

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_016628.5(WAC):c.367A>C (p.Lys123Gln) rs949649739 0.00002
NM_001002295.2(GATA3):c.71C>T (p.Pro24Leu) rs1485724723 0.00001
GRCh37/hg19 10q24.31-24.32(chr10:102822575-103558868)
GRCh37/hg19 10q25.3-26.13(chr10:117024753-124942806)
NM_001002295.2(GATA3):c.639_648del (p.Ser214fs)
NM_016628.5(WAC):c.1101dup (p.Pro368fs) rs1841061596
NM_016628.5(WAC):c.310del (p.His104fs) rs1589196229

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