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rs398123165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs398123165(-;-)
Make rs398123165(-;AAAG)
ReferenceGRCh38 38.1/141
Chromosome1
Position241497912
GeneFH
is asnp
is mentioned by
dbSNPrs398123165
ebirs398123165
HLIrs398123165
Exacrs398123165
Varsomers398123165
Maprs398123165
PheGenIrs398123165
hapmaprs398123165
1000 genomesrs398123165
hgdprs398123165
ensemblrs398123165
gopubmedrs398123165
geneviewrs398123165
scholarrs398123165
googlers398123165
pharmgkbrs398123165
gwascentralrs398123165
openSNPrs398123165
23andMers398123165
23andMe allrs398123165
SNP Nexus

SNPshotrs398123165
SNPdbers398123165
MSV3drs398123165
GWAS Ctlgrs398123165
Max Magnitude0
ClinVar
Risk rs398123165(;)
Alt rs398123165(;)
Reference rs398123165(AAAG;AAAG)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241661212_241661215delCTTT
CLNSRC ClinVar
CLNACC RCV000078147.4,