ClinVar Miner

List of variants in gene LOC129935618, WNT10A studied for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_025216.2(WNT10A):c.-400T>G rs556182426 0.00738
NM_025216.2(WNT10A):c.-312C>T rs138370318 0.00068
NM_025216.2(WNT10A):c.-341A>G rs762914440 0.00029
NM_025216.2(WNT10A):c.-270G>C rs774035749 0.00010
NM_025216.2(WNT10A):c.-285C>T rs886055636 0.00002
NM_025216.2(WNT10A):c.-249G>C rs571829301
NM_025216.2(WNT10A):c.-358G>A rs886055635
NM_025216.2(WNT10A):c.-370C>A rs886055634
NM_025216.2(WNT10A):c.-433C>G rs886055633

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