ClinVar Miner

List of variants in gene DCPS, TIRAP studied for autosomal recessive non-syndromic intellectual disability

Included ClinVar conditions (71):
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_014026.6(DCPS):c.189C>T (p.Phe63=) rs695029 0.19665
NM_014026.6(DCPS):c.87G>T (p.Glu29Asp) rs147935593 0.00061
NM_014026.6(DCPS):c.201+4C>G rs746334180 0.00001
NM_014026.6(DCPS):c.201+1G>T
NM_014026.6(DCPS):c.201+2T>C rs1057519083

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