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rs398123168

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123168(C;T)
Make rs398123168(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position241504198
GeneFH
is asnp
is mentioned by
dbSNPrs398123168
ebirs398123168
HLIrs398123168
Exacrs398123168
Varsomers398123168
Maprs398123168
PheGenIrs398123168
hapmaprs398123168
1000 genomesrs398123168
hgdprs398123168
ensemblrs398123168
gopubmedrs398123168
geneviewrs398123168
scholarrs398123168
googlers398123168
pharmgkbrs398123168
gwascentralrs398123168
openSNPrs398123168
23andMers398123168
23andMe allrs398123168
SNP Nexus

SNPshotrs398123168
SNPdbers398123168
MSV3drs398123168
GWAS Ctlgrs398123168
Max Magnitude0
ClinVar
Risk rs398123168(T;T)
Alt rs398123168(T;T)
Reference rs398123168(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241667498G>A
CLNSRC HGMD
CLNACC RCV000078152.5,