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rs1057524385

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524385(C;G)
Make rs1057524385(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241504227
GeneFH
is asnp
is mentioned by
dbSNPrs1057524385
dbSNP (old)rs1057524385
ClinGenrs1057524385
ebirs1057524385
HLIrs1057524385
Exacrs1057524385
Gnomadrs1057524385
Varsomers1057524385
Maprs1057524385
PheGenIrs1057524385
Biobankrs1057524385
1000 genomesrs1057524385
hgdprs1057524385
ensemblrs1057524385
gopubmedrs1057524385
geneviewrs1057524385
scholarrs1057524385
googlers1057524385
pharmgkbrs1057524385
gwascentralrs1057524385
openSNPrs1057524385
23andMers1057524385
23andMe allrs1057524385
SNPshotrs1057524385
SNPdbers1057524385
MSV3drs1057524385
GWAS Ctlgrs1057524385
Max Magnitude0
ClinVar
Risk rs1057524385(G;G)
Alt rs1057524385(G;G)
Reference Rs1057524385(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667527G>C
CLNSRC
CLNACC RCV000430394.1,