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rs1057517734

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517734(G;T)
Make rs1057517734(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241504041
GeneFH
is asnp
is mentioned by
dbSNPrs1057517734
dbSNP (old)rs1057517734
ClinGenrs1057517734
ebirs1057517734
HLIrs1057517734
Exacrs1057517734
Gnomadrs1057517734
Varsomers1057517734
Maprs1057517734
PheGenIrs1057517734
Biobankrs1057517734
1000 genomesrs1057517734
hgdprs1057517734
ensemblrs1057517734
gopubmedrs1057517734
geneviewrs1057517734
scholarrs1057517734
googlers1057517734
pharmgkbrs1057517734
gwascentralrs1057517734
openSNPrs1057517734
23andMers1057517734
23andMe allrs1057517734
SNPshotrs1057517734
SNPdbers1057517734
MSV3drs1057517734
GWAS Ctlgrs1057517734
Max Magnitude0
ClinVar
Risk rs1057517734(T;T)
Alt rs1057517734(T;T)
Reference Rs1057517734(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667341C>A
CLNSRC
CLNACC RCV000414171.1,