FAM222A Chromosome 12

Family with sequence similarity 222 member A
1 variant 1 Health Risk

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What This Gene Does
"CLNSIG=4
Associated Conditions (1)
Abnormal brain morphology
Key Variants
RS763757845
Likely pathogenic
Abnormal brain morphology, Abnormal brain morphology
Health Risk
All Variants (1)
RSID Category Clinical Significance Conditions
RS763757845 Health Risk Likely pathogenic Abnormal brain morphology, Abnormal brain morphology
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