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Items: 2

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr1:213031948
GRCh38:
Chr1:212858606
FLVCR1not specifiedGO-ESP:0.39456(C)
GMAF:0.44450(C)
Likely benignno assertion criteria provided
2.
GRCh37:
Chr1:213068595
GRCh38:
Chr1:212895253
FLVCR1not specifiedGO-ESP:0.38490(T)
GMAF:0.37940(T)
Likely benignno assertion criteria provided