ClinVar Miner

List of variants in gene IGH, IGHM studied for B cell deficiency

Included ClinVar conditions (64):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NC_000014.9:g.105855041A>G rs10287 0.05231
NC_000014.9:g.105855988G>C rs113762053 0.04825
NC_000014.9:g.105854900G>T rs373184157 0.00003
NC_000014.9:g.105854405C>T rs376256147 0.00002
NC_000014.9:g.105854468A>C rs267606871
NC_000014.9:g.105855107C>T rs281865422
NC_000014.9:g.105855132dup rs2092930640
NC_000014.9:g.105855203G>A
NC_000014.9:g.105855623_105855624del
NC_000014.9:g.105856013G>T rs2142904095
NC_000014.9:g.105856087G>A rs2142904392
NC_000014.9:g.105856156C>T rs201981439

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