ClinVar Miner

List of variants in gene FANCB reported as benign for X-linked syndromic intellectual disability

Included ClinVar conditions (165):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_001018113.2(FANCB):c.1327-3delT rs202067682
NM_001018113.3(FANCB):c.*14T>C rs2375726
NM_001018113.3(FANCB):c.-173G>C rs2188383
NM_001018113.3(FANCB):c.-229T>G rs149617434
NM_001018113.3(FANCB):c.1004G>A (p.Gly335Glu) rs41309679
NM_001018113.3(FANCB):c.1327-10T>C rs2905223

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