Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123160

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123160(C;T)
Make rs398123160(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position241502553
GeneFH
is asnp
is mentioned by
dbSNPrs398123160
ebirs398123160
HLIrs398123160
Exacrs398123160
Varsomers398123160
Maprs398123160
PheGenIrs398123160
hapmaprs398123160
1000 genomesrs398123160
hgdprs398123160
ensemblrs398123160
gopubmedrs398123160
geneviewrs398123160
scholarrs398123160
googlers398123160
pharmgkbrs398123160
gwascentralrs398123160
openSNPrs398123160
23andMers398123160
23andMe allrs398123160
SNP Nexus

SNPshotrs398123160
SNPdbers398123160
MSV3drs398123160
GWAS Ctlgrs398123160
Max Magnitude0
ClinVar
Risk rs398123160(T;T)
Alt rs398123160(T;T)
Reference rs398123160(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241665853G>A
CLNSRC ClinVar Emory University
CLNACC RCV000078141.4,