ClinVar Miner

List of variants in gene ATP2A1, ATXN2L, EIF3C, NUPR1, SGF29, SH2B1, SULT1A1, SULT1A2, TUFM studied for syndrome caused by partial chromosomal deletion

Included ClinVar conditions (110):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 16p11.2(chr16:28529940-28906458)

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