ClinVar Miner

List of variants in gene LFNG, LOC129997823 studied for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_001040167.2(LFNG):c.75C>T (p.Thr25=) rs767338996 0.00209
NM_001040167.2(LFNG):c.37C>G (p.Leu13Val) rs1425455790 0.00007
NM_001040167.2(LFNG):c.6C>A (p.Leu2=) rs1390203183 0.00003
NM_001040167.2(LFNG):c.57C>T (p.Ala19=) rs1779736182 0.00001
NM_001040167.2(LFNG):c.10C>G (p.Arg4Gly) rs1341252096
NM_001040167.2(LFNG):c.10C>T (p.Arg4Cys)
NM_001040167.2(LFNG):c.41C>G (p.Ala14Gly)
NM_001040167.2(LFNG):c.46G>A (p.Ala16Thr) rs1779735531
NM_001040167.2(LFNG):c.67G>T (p.Val23Leu) rs2128375068
NM_001040167.2(LFNG):c.84G>T (p.Pro28=)

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