ClinVar Miner

List of variants in gene SFRP4 studied for bone development disease

Included ClinVar conditions (588):
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Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_003014.4(SFRP4):c.786C>T (p.Arg262=) rs1132553 0.54626
NM_003014.4(SFRP4):c.567G>A (p.Thr189=) rs1132552 0.43818
NM_003014.4(SFRP4):c.958C>A (p.Pro320Thr) rs1802073 0.43676
NM_003014.4(SFRP4):c.1019G>A (p.Arg340Lys) rs1802074 0.24674
NM_003014.4(SFRP4):c.566C>T (p.Thr189Met) rs149860855 0.00031
NM_003014.3(SFRP4):c.694C>T rs755007671
NM_003014.4(SFRP4):c.161C>A (p.Ala54Asp) rs758308395
NM_003014.4(SFRP4):c.373T>A (p.Cys125Ser) rs1344808304
NM_003014.4(SFRP4):c.481_487del (p.Val161fs) rs879253778
NM_003014.4(SFRP4):c.499dup (p.Asp167fs) rs879255603

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