ClinVar Miner

List of variants in gene FLRT3, MACROD2 studied for Kallmann syndrome

Included ClinVar conditions (26):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_198391.3(FLRT3):c.1257C>T (p.Thr419=) rs6042672 0.31273
NM_198391.3(FLRT3):c.1255A>T (p.Thr419Ser) rs769008665 0.00009
NM_198391.3(FLRT3):c.1016A>G (p.Lys339Arg) rs398124654
NM_198391.3(FLRT3):c.1727C>T (p.Ala576Val)
NM_198391.3(FLRT3):c.999G>A (p.Met333Ile)

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