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rs398123162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123162(-;-)
Make rs398123162(-;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position241502479
GeneFH
is asnp
is mentioned by
dbSNPrs398123162
ebirs398123162
HLIrs398123162
Exacrs398123162
Varsomers398123162
Maprs398123162
PheGenIrs398123162
hapmaprs398123162
1000 genomesrs398123162
hgdprs398123162
ensemblrs398123162
gopubmedrs398123162
geneviewrs398123162
scholarrs398123162
googlers398123162
pharmgkbrs398123162
gwascentralrs398123162
openSNPrs398123162
23andMers398123162
23andMe allrs398123162
SNP Nexus

SNPshotrs398123162
SNPdbers398123162
MSV3drs398123162
GWAS Ctlgrs398123162
Max Magnitude0
ClinVar
Risk rs398123162(;)
Alt rs398123162(;)
Reference rs398123162(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241665779delA
CLNSRC ClinVar
CLNACC RCV000078143.4,