ClinVar Miner

List of variants in gene NSMF studied for Kallmann syndrome

Included ClinVar conditions (26):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_001130969.3(NSMF):c.586C>T (p.Arg196Cys) rs776491850 0.00004
NM_001130969.3(NSMF):c.1132-22_1132-15del rs751029049
NM_001130969.3(NSMF):c.1132-23_1132-15del rs606231136
NM_001130969.3(NSMF):c.194C>A (p.Pro65His)

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