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rs398123167

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123167(C;T)
Make rs398123167(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position241506147
GeneFH
is asnp
is mentioned by
dbSNPrs398123167
ebirs398123167
HLIrs398123167
Exacrs398123167
Varsomers398123167
Maprs398123167
PheGenIrs398123167
hapmaprs398123167
1000 genomesrs398123167
hgdprs398123167
ensemblrs398123167
gopubmedrs398123167
geneviewrs398123167
scholarrs398123167
googlers398123167
pharmgkbrs398123167
gwascentralrs398123167
openSNPrs398123167
23andMers398123167
23andMe allrs398123167
SNP Nexus

SNPshotrs398123167
SNPdbers398123167
MSV3drs398123167
GWAS Ctlgrs398123167
Max Magnitude0
ClinVar
Risk rs398123167(T;T)
Alt rs398123167(T;T)
Reference rs398123167(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241669447G>A
CLNSRC ClinVar Emory University
CLNACC RCV000078151.4,