ClinVar Miner

List of variants in gene PRMT7 reported as benign for short stature-brachydactyly-obesity-global developmental delay syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_019023.5(PRMT7):c.1797C>T (p.Thr599=) rs1131933 0.48912
NM_019023.5(PRMT7):c.1638C>T (p.Asp546=) rs61746794 0.13248
NM_019023.5(PRMT7):c.1276-18G>A rs7190134 0.13231
NM_019023.5(PRMT7):c.1905C>T (p.Pro635=) rs61733486 0.06161
NM_019023.5(PRMT7):c.1650+27A>C rs1868159

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