ClinVar Miner

List of variants studied for HSD10 disease, atypical type by Neuberg Centre For Genomic Medicine, NCGM

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_004493.3(HSD17B10):c.113T>C (p.Val38Ala)
NM_004493.3(HSD17B10):c.11C>G (p.Ala4Gly)
NM_004493.3(HSD17B10):c.62G>T (p.Gly21Val)

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