ClinVar Miner

List of variants in gene PIGV reported as benign for congenital limb malformation

Included ClinVar conditions (335):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_017837.4(PIGV):c.-338A>C rs113400508 0.05897
NM_017837.4(PIGV):c.*210A>G rs57189461 0.05712
NM_017837.4(PIGV):c.615C>T (p.Asn205=) rs34512715 0.00995
NM_017837.4(PIGV):c.101C>T (p.Pro34Leu) rs139246652 0.00505
NM_017837.4(PIGV):c.*167G>A rs142176099 0.00264
NM_017837.4(PIGV):c.*149G>A rs3754360 0.00091
NM_017837.4(PIGV):c.-333C>T rs118069986

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