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rs201261794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201261794(A;T)
Make rs201261794(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241519721
GeneFH
is asnp
is mentioned by
dbSNPrs201261794
dbSNP (old)rs201261794
ClinGenrs201261794
ebirs201261794
HLIrs201261794
Exacrs201261794
Gnomadrs201261794
Varsomers201261794
Maprs201261794
PheGenIrs201261794
Biobankrs201261794
1000 genomesrs201261794
hgdprs201261794
ensemblrs201261794
gopubmedrs201261794
geneviewrs201261794
scholarrs201261794
googlers201261794
pharmgkbrs201261794
gwascentralrs201261794
openSNPrs201261794
23andMers201261794
23andMe allrs201261794
SNPshotrs201261794
SNPdbers201261794
MSV3drs201261794
GWAS Ctlgrs201261794
Max Magnitude0
ClinVar
Risk rs201261794(G;G) rs201261794(T;T)
Alt rs201261794(G;G) rs201261794(T;T)
Reference Rs201261794(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.241683021A>C
CLNSRC
CLNACC RCV000493638.1,