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rs794726669

From SNPedia

ClinVar
Risk rs794726669(;)
Alt rs794726669(;)
Reference rs794726669(TTGGAG;TTGGAG)
Significance Pathogenic
Disease Apparent mineralocorticoid excess
Variation info
Gene HSD11B2
CLNDBN Apparent mineralocorticoid excess, mild
Reversed 0
HGVS NC_000016.9:g.67469608_67469613delGAGTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000012882.4,