Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs11545655

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11545655(C;C)
Make rs11545655(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241504129
GeneFH
is asnp
is mentioned by
dbSNPrs11545655
dbSNP (old)rs11545655
ClinGenrs11545655
ebirs11545655
HLIrs11545655
Exacrs11545655
Gnomadrs11545655
Varsomers11545655
Maprs11545655
PheGenIrs11545655
Biobankrs11545655
1000 genomesrs11545655
hgdprs11545655
ensemblrs11545655
gopubmedrs11545655
geneviewrs11545655
scholarrs11545655
googlers11545655
pharmgkbrs11545655
gwascentralrs11545655
openSNPrs11545655
23andMers11545655
23andMe allrs11545655
SNPshotrs11545655
SNPdbers11545655
MSV3drs11545655
GWAS Ctlgrs11545655
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs11545655(A;A) rs11545655(C;C)
Alt rs11545655(A;A) rs11545655(C;C)
Reference Rs11545655(G;G)
Significance Probable-Pathogenic
Disease Fumarase deficiency
Variation info
Gene FH
CLNDBN Fumarase deficiency
Reversed 1
HGVS NC_000001.10:g.241667429C>T
CLNSRC
CLNACC RCV000472953.1,