ClinVar Miner

List of variants reported as benign for tooth and nail syndrome by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_002448.3(MSX1):c.*276A>G rs12532 0.36320
NM_002448.3(MSX1):c.*6C>T rs8670 0.22915
NM_002448.3(MSX1):c.119C>G (p.Ala40Gly) rs36059701 0.14189
NM_002448.3(MSX1):c.348C>T (p.Gly116=) rs34165410 0.05963
NM_002448.3(MSX1):c.561G>A (p.Leu187=) rs149960650 0.00512
NM_002448.3(MSX1):c.218C>T (p.Pro73Leu) rs201156596 0.00425
NM_002448.3(MSX1):c.86C>T (p.Ala29Val) rs530217423 0.00336
NM_002448.3(MSX1):c.297G>C (p.Pro99=) rs757688467 0.00081
NM_002448.3(MSX1):c.151A>G (p.Lys51Glu) rs994158401 0.00018
NM_002448.3(MSX1):c.127A>C (p.Met43Leu) rs565664559 0.00007
NM_002448.3(MSX1):c.260A>G (p.Gln87Arg)
NM_002448.3(MSX1):c.469+46_469+56del rs149370601
NM_002448.3(MSX1):c.471G>T (p.Arg157Ser) rs150284621

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