ClinVar Miner

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

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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NM_198270.4(NHS):c.2214T>C (p.Tyr738=) rs1323986389
NM_198270.4(NHS):c.2824C>T (p.Leu942=)
NM_198270.4(NHS):c.2846C>T (p.Thr949Met) rs373464879
NM_198270.4(NHS):c.3030G>A (p.Thr1010=) rs1157246576
NM_198270.4(NHS):c.3723G>A (p.Thr1241=) rs150235442
NM_198270.4(NHS):c.408C>T (p.Leu136=) rs1555981412
NM_198270.4(NHS):c.903G>A (p.Pro301=)

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