Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913051

From SNPedia

OMIM134370
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913051(G,T;G,T)
Alt rs121913051(G,T;G,T)
Reference rs121913051(C;C)
Significance Other
Disease Atypical hemolytic-uremic syndrome 1
Variation info
Gene CFH
CLNDBN Atypical hemolytic-uremic syndrome 1
Reversed 0
HGVS NC_000001.10:g.196716390C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018008.2,