ClinVar Miner

List of variants in gene WIPF1 reported as benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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NM_001077269.1(WIPF1):c.1164C>T (p.Asn388=) rs41270199
NM_001077269.1(WIPF1):c.1227T>C (p.Ser409=) rs577852991
NM_001077269.1(WIPF1):c.1296A>G (p.Pro432=) rs76731102
NM_001077269.1(WIPF1):c.1413G>A (p.Thr471=) rs149092210
NM_001077269.1(WIPF1):c.1446C>T (p.Asn482=) rs116757787
NM_001077269.1(WIPF1):c.208G>A (p.Gly70Ser) rs138276021
NM_001077269.1(WIPF1):c.339C>G (p.Ser113=) rs76308107
NM_001077269.1(WIPF1):c.42G>A (p.Thr14=) rs111761533
NM_001077269.1(WIPF1):c.593C>T (p.Pro198Leu) rs4972450
NM_001077269.1(WIPF1):c.78T>C (p.Asn26=) rs35923393

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